Canonical Allele Identifier: CA435431467

Gene: MYLK MYLK-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123614207G>C , CM000665.2:g.123614207G>C	GRCh38
NC_000003.11:g.123333054G>C , CM000665.1:g.123333054G>C	GRCh37
NC_000003.10:g.124815744G>C	NCBI36
NG_029111.1:g.275096C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346322.10:c.5283C>G (MYLK)	ENSP00000320622.6:p.Thr1761=
ENST00000508240.2:c.2043C>G (MYLK)	ENSP00000422984.2:p.Thr681=
ENST00000578202.2:c.*148C>G (MYLK)	ENSP00000463691.2:n.*148C>G
ENST00000583087.6:c.363C>G (MYLK)	ENSP00000462118.1:p.Thr121=
ENST00000685021.1:c.2877C>G (MYLK)	ENSP00000508447.1:p.Thr959=
ENST00000685170.1:n.856C>G (MYLK)
ENST00000685259.1:c.3162C>G (MYLK)
ENST00000685744.1:c.360C>G (MYLK)	ENSP00000510047.1:p.Thr120=
ENST00000685907.1:n.3424C>G (MYLK)
ENST00000685953.1:c.2040C>G (MYLK)	ENSP00000510593.1:p.Thr680=
ENST00000686039.1:c.3027C>G (MYLK)
ENST00000686245.1:c.2760C>G (MYLK)	ENSP00000509313.1:p.Thr920=
ENST00000686281.1:n.935C>G (MYLK)
ENST00000686406.1:c.5640C>G (MYLK)	ENSP00000509044.1:p.Thr1880=
ENST00000686458.1:n.2145C>G (MYLK)
ENST00000686761.1:c.5643C>G (MYLK)	ENSP00000508758.1:p.Thr1881=
ENST00000687375.1:c.360C>G (MYLK)	ENSP00000509867.1:p.Thr120=
ENST00000687434.1:c.*1859C>G (MYLK)	ENSP00000509751.1:n.*1859C>G
ENST00000687709.1:n.3698C>G (MYLK)
ENST00000687848.1:c.5673C>G (MYLK)	ENSP00000508761.1:p.Thr1891=
ENST00000688024.1:c.2874C>G (MYLK)	ENSP00000509803.1:p.Thr958=
ENST00000688223.1:c.2673C>G (MYLK)	ENSP00000508935.1:p.Thr891=
ENST00000689446.1:n.845C>G (MYLK)
ENST00000689868.1:n.5903C>G (MYLK)
ENST00000689918.1:n.1718C>G (MYLK)
ENST00000690167.1:n.3311C>G (MYLK)
ENST00000690457.1:c.4881C>G (MYLK)	ENSP00000508777.1:p.Thr1627=
ENST00000690656.1:n.348C>G (MYLK)
ENST00000691367.1:n.339C>G (MYLK)
ENST00000691933.1:c.3267C>G (MYLK)
ENST00000692356.1:c.89-95C>G (MYLK)	ENSP00000509805.1:n.89-95C>G
ENST00000692507.1:n.1447C>G (MYLK)
ENST00000693689.1:c.5436C>G (MYLK)	ENSP00000510503.1:p.Thr1812=
ENST00000360304.8:c.5643C>G (MYLK) MANE Select	ENSP00000353452.3:p.Thr1881=
ENST00000346322.9:c.5436C>G (MYLK)	ENSP00000320622.5:p.Thr1812=
ENST00000354792.9:c.5436C>G (MYLK)	ENSP00000346846.6:p.Thr1812=
ENST00000359169.5:c.5490C>G (MYLK)	ENSP00000352088.1:p.Thr1830=
ENST00000360304.7:c.5643C>G (MYLK)	ENSP00000353452.3:p.Thr1881=
ENST00000360772.7:c.5490C>G (MYLK)	ENSP00000354004.3:p.Thr1830=
ENST00000418370.6:c.363C>G (MYLK)	ENSP00000428967.1:p.Thr121=
ENST00000464489.5:c.*5222C>G (MYLK)	ENSP00000417798.1:n.*5222C>G
ENST00000475616.5:c.5643C>G (MYLK)	ENSP00000418335.1:p.Thr1881=
ENST00000578202.1:c.360C>G (MYLK)	ENSP00000463691.1:p.Thr120=
ENST00000583087.5:c.363C>G (MYLK)	ENSP00000462118.1:p.Thr121=
NM_053025.3:c.5643C>G (MYLK)	NP_444253.3:p.Thr1881=
NM_053026.3:c.5436C>G (MYLK)	NP_444254.3:p.Thr1812=
NM_053027.3:c.5490C>G (MYLK)	NP_444255.3:p.Thr1830=
NM_053028.3:c.5283C>G (MYLK)	NP_444256.3:p.Thr1761=
NM_053031.2:c.360C>G (MYLK)	NP_444259.1:p.Thr120=
NM_053032.2:c.363C>G (MYLK)	NP_444260.1:p.Thr121=
NR_038266.2:n.290-15287G>C (MYLK-AS1)
NR_121654.1:n.197-15287G>C (MYLK-AS1)
XM_011512860.1:c.5640C>G (MYLK)	XP_011511162.1:p.Thr1880=
XM_011512861.1:c.5439C>G (MYLK)	XP_011511163.1:p.Thr1813=
XM_011512862.1:c.5115C>G (MYLK)	XP_011511164.1:p.Thr1705=
NM_001321309.1:c.5115C>G (MYLK)	NP_001308238.1:p.Thr1705=
NM_053031.3:c.360C>G (MYLK)	NP_444259.1:p.Thr120=
NM_053032.3:c.363C>G (MYLK)	NP_444260.1:p.Thr121=
XM_011512860.3:c.5670C>G (MYLK)	XP_011511162.2:p.Thr1890=
XM_011512861.3:c.5469C>G (MYLK)	XP_011511163.2:p.Thr1823=
XM_017006469.2:c.2874C>G (MYLK)	XP_016861958.1:p.Thr958=
XM_017006470.2:c.2040C>G (MYLK)	XP_016861959.1:p.Thr680=
XM_017006471.2:c.2043C>G (MYLK)	XP_016861960.1:p.Thr681=
XM_017006472.2:c.363C>G (MYLK)	XP_016861961.1:p.Thr121=
XM_017006473.1:c.360C>G (MYLK)	XP_016861962.1:p.Thr120=
XM_024453532.1:c.5673C>G (MYLK)	XP_024309300.1:p.Thr1891=
XM_024453533.1:c.5643C>G (MYLK)	XP_024309301.1:p.Thr1881=
XM_024453534.1:c.5466C>G (MYLK)	XP_024309302.1:p.Thr1822=
XM_024453535.1:c.5436C>G (MYLK)	XP_024309303.1:p.Thr1812=
XM_024453536.1:c.5643C>G (MYLK)	XP_024309304.1:p.Thr1881=
XM_024453537.1:c.5643C>G (MYLK)	XP_024309305.1:p.Thr1881=
NM_001321309.2:c.5115C>G (MYLK)	NP_001308238.1:p.Thr1705=
NM_053025.4:c.5643C>G (MYLK) MANE Select	NP_444253.3:p.Thr1881=
NM_053026.4:c.5436C>G (MYLK)	NP_444254.3:p.Thr1812=
NM_053027.4:c.5490C>G (MYLK)	NP_444255.3:p.Thr1830=
NM_053028.4:c.5283C>G (MYLK)	NP_444256.3:p.Thr1761=
NM_053031.4:c.360C>G (MYLK)	NP_444259.1:p.Thr120=
NM_053032.4:c.363C>G (MYLK)	NP_444260.1:p.Thr121=