Canonical Allele Identifier: CA1139658241

Gene: MYLK MYLK-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123614051T>C , CM000665.2:g.123614051T>C	GRCh38
NC_000003.11:g.123332898T>C , CM000665.1:g.123332898T>C	GRCh37
NC_000003.10:g.124815588T>C	NCBI36
NG_029111.1:g.275252A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346322.10:c.*54A>G (MYLK)	ENSP00000320622.6:n.*54A>G
ENST00000508240.2:c.*54A>G (MYLK)	ENSP00000422984.2:n.*54A>G
ENST00000578202.2:c.*304A>G (MYLK)	ENSP00000463691.2:n.*304A>G
ENST00000583087.6:c.*54A>G (MYLK)	ENSP00000462118.1:n.*54A>G
ENST00000685021.1:c.*54A>G (MYLK)	ENSP00000508447.1:n.*54A>G
ENST00000685170.1:n.1012A>G (MYLK)
ENST00000685744.1:c.*54A>G (MYLK)	ENSP00000510047.1:n.*54A>G
ENST00000685953.1:c.*54A>G (MYLK)	ENSP00000510593.1:n.*54A>G
ENST00000686039.1:c.3183A>G (MYLK)
ENST00000686281.1:n.1091A>G (MYLK)
ENST00000686458.1:n.2301A>G (MYLK)
ENST00000686761.1:c.*54A>G (MYLK)	ENSP00000508758.1:n.*54A>G
ENST00000687434.1:c.*2015A>G (MYLK)	ENSP00000509751.1:n.*2015A>G
ENST00000688024.1:c.*54A>G (MYLK)	ENSP00000509803.1:n.*54A>G
ENST00000688223.1:c.*54A>G (MYLK)	ENSP00000508935.1:n.*54A>G
ENST00000689446.1:n.1001A>G (MYLK)
ENST00000689868.1:n.6059A>G (MYLK)
ENST00000690167.1:n.3467A>G (MYLK)
ENST00000690656.1:n.504A>G (MYLK)
ENST00000691367.1:n.495A>G (MYLK)
ENST00000691933.1:c.3423A>G (MYLK)
ENST00000692356.1:c.*54A>G (MYLK)	ENSP00000509805.1:n.*54A>G
ENST00000692507.1:n.1603A>G (MYLK)
ENST00000693689.1:c.*54A>G (MYLK)	ENSP00000510503.1:n.*54A>G
ENST00000360304.8:c.*54A>G (MYLK) MANE Select	ENSP00000353452.3:n.*54A>G
ENST00000346322.9:c.*54A>G (MYLK)	ENSP00000320622.5:n.*54A>G
ENST00000354792.9:c.*54A>G (MYLK)	ENSP00000346846.6:n.*54A>G
ENST00000359169.5:c.*54A>G (MYLK)	ENSP00000352088.1:n.*54A>G
ENST00000360304.7:c.*54A>G (MYLK)	ENSP00000353452.3:n.*54A>G
ENST00000360772.7:c.*54A>G (MYLK)	ENSP00000354004.3:n.*54A>G
ENST00000418370.6:c.*54A>G (MYLK)	ENSP00000428967.1:n.*54A>G
ENST00000464489.5:c.*5378A>G (MYLK)	ENSP00000417798.1:n.*5378A>G
ENST00000578202.1:c.*54A>G (MYLK)	ENSP00000463691.1:n.*54A>G
NM_053025.3:c.*54A>G (MYLK)	NP_444253.3:n.*54A>G
NM_053026.3:c.*54A>G (MYLK)	NP_444254.3:n.*54A>G
NM_053027.3:c.*54A>G (MYLK)	NP_444255.3:n.*54A>G
NM_053028.3:c.*54A>G (MYLK)	NP_444256.3:n.*54A>G
NM_053031.2:c.*54A>G (MYLK)	NP_444259.1:n.*54A>G
NM_053032.2:c.*54A>G (MYLK)	NP_444260.1:n.*54A>G
NR_038266.2:n.290-15443T>C (MYLK-AS1)
NR_121654.1:n.197-15443T>C (MYLK-AS1)
XM_011512860.1:c.*54A>G (MYLK)	XP_011511162.1:n.*54A>G
XM_011512861.1:c.*54A>G (MYLK)	XP_011511163.1:n.*54A>G
XM_011512862.1:c.*54A>G (MYLK)	XP_011511164.1:n.*54A>G
NM_001321309.1:c.*54A>G (MYLK)	NP_001308238.1:n.*54A>G
NM_053031.3:c.*54A>G (MYLK)	NP_444259.1:n.*54A>G
NM_053032.3:c.*54A>G (MYLK)	NP_444260.1:n.*54A>G
XM_011512860.3:c.*54A>G (MYLK)	XP_011511162.2:n.*54A>G
XM_011512861.3:c.*54A>G (MYLK)	XP_011511163.2:n.*54A>G
XM_017006469.2:c.*54A>G (MYLK)	XP_016861958.1:n.*54A>G
XM_017006470.2:c.*54A>G (MYLK)	XP_016861959.1:n.*54A>G
XM_017006471.2:c.*54A>G (MYLK)	XP_016861960.1:n.*54A>G
XM_017006472.2:c.*54A>G (MYLK)	XP_016861961.1:n.*54A>G
XM_017006473.1:c.*54A>G (MYLK)	XP_016861962.1:n.*54A>G
XM_024453532.1:c.*54A>G (MYLK)	XP_024309300.1:n.*54A>G
XM_024453533.1:c.*54A>G (MYLK)	XP_024309301.1:n.*54A>G
XM_024453534.1:c.*54A>G (MYLK)	XP_024309302.1:n.*54A>G
XM_024453535.1:c.*54A>G (MYLK)	XP_024309303.1:n.*54A>G
XM_024453536.1:c.*54A>G (MYLK)	XP_024309304.1:n.*54A>G
XM_024453537.1:c.*54A>G (MYLK)	XP_024309305.1:n.*54A>G
NM_001321309.2:c.*54A>G (MYLK)	NP_001308238.1:n.*54A>G
NM_053025.4:c.*54A>G (MYLK) MANE Select	NP_444253.3:n.*54A>G
NM_053026.4:c.*54A>G (MYLK)	NP_444254.3:n.*54A>G
NM_053027.4:c.*54A>G (MYLK)	NP_444255.3:n.*54A>G
NM_053028.4:c.*54A>G (MYLK)	NP_444256.3:n.*54A>G
NM_053031.4:c.*54A>G (MYLK)	NP_444259.1:n.*54A>G
NM_053032.4:c.*54A>G (MYLK)	NP_444260.1:n.*54A>G