Canonical Allele Identifier: CA435298779

Gene: MYLK

Linked Data

• MyVariant Identifiers: chr3:g.123366133A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123647286A>T , CM000665.2:g.123647286A>T	GRCh38
NC_000003.11:g.123366133A>T , CM000665.1:g.123366133A>T	GRCh37
NC_000003.10:g.124848823A>T	NCBI36
NG_029111.1:g.242017T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346322.10:c.4350T>A	ENSP00000320622.6:p.Pro1450=
ENST00000508240.2:c.957T>A	ENSP00000422984.2:p.Pro319=
ENST00000513111.2:n.687T>A
ENST00000684879.1:n.2189T>A
ENST00000685021.1:c.1791T>A	ENSP00000508447.1:p.Pro597=
ENST00000685259.1:c.2076T>A
ENST00000685907.1:n.2338T>A
ENST00000685953.1:c.957T>A	ENSP00000510593.1:p.Pro319=
ENST00000686039.1:c.1941T>A
ENST00000686245.1:c.1674T>A	ENSP00000509313.1:p.Pro558=
ENST00000686406.1:c.4557T>A	ENSP00000509044.1:p.Pro1519=
ENST00000686458.1:n.1059T>A
ENST00000686761.1:c.4557T>A	ENSP00000508758.1:p.Pro1519=
ENST00000686822.1:n.4451T>A
ENST00000687434.1:c.*773T>A	ENSP00000509751.1:n.*773T>A
ENST00000687709.1:n.2612T>A
ENST00000687848.1:c.4587T>A	ENSP00000508761.1:p.Pro1529=
ENST00000688024.1:c.1791T>A	ENSP00000509803.1:p.Pro597=
ENST00000688223.1:c.1649+1685T>A	ENSP00000508935.1:n.1649+1685T>A
ENST00000689868.1:n.2285T>A
ENST00000689918.1:n.632T>A
ENST00000690086.1:n.658T>A
ENST00000690167.1:n.2228T>A
ENST00000690457.1:c.3795T>A	ENSP00000508777.1:p.Pro1265=
ENST00000690534.1:n.1078T>A
ENST00000691933.1:c.2181T>A
ENST00000692352.1:c.2095T>A
ENST00000693689.1:c.4350T>A	ENSP00000510503.1:p.Pro1450=
ENST00000360304.8:c.4557T>A MANE Select	ENSP00000353452.3:p.Pro1519=
ENST00000346322.9:c.4350T>A	ENSP00000320622.5:p.Pro1450=
ENST00000354792.9:c.4350T>A	ENSP00000346846.6:p.Pro1450=
ENST00000359169.5:c.4557T>A	ENSP00000352088.1:p.Pro1519=
ENST00000360304.7:c.4557T>A	ENSP00000353452.3:p.Pro1519=
ENST00000360772.7:c.4557T>A	ENSP00000354004.3:p.Pro1519=
ENST00000464489.5:c.*4136T>A	ENSP00000417798.1:n.*4136T>A
ENST00000475616.5:c.4557T>A	ENSP00000418335.1:p.Pro1519=
ENST00000513111.1:n.269T>A
ENST00000514895.5:n.94+1685T>A
NM_053025.3:c.4557T>A	NP_444253.3:p.Pro1519=
NM_053026.3:c.4350T>A	NP_444254.3:p.Pro1450=
NM_053027.3:c.4557T>A	NP_444255.3:p.Pro1519=
NM_053028.3:c.4350T>A	NP_444256.3:p.Pro1450=
XM_011512860.1:c.4557T>A	XP_011511162.1:p.Pro1519=
XM_011512861.1:c.4415+1685T>A	XP_011511163.1:n.4415+1685T>A
XM_011512862.1:c.4029T>A	XP_011511164.1:p.Pro1343=
NM_001321309.1:c.4029T>A	NP_001308238.1:p.Pro1343=
XM_011512860.3:c.4587T>A	XP_011511162.2:p.Pro1529=
XM_011512861.3:c.4445+1685T>A	XP_011511163.2:n.4445+1685T>A
XM_017006469.2:c.1791T>A	XP_016861958.1:p.Pro597=
XM_017006470.2:c.957T>A	XP_016861959.1:p.Pro319=
XM_017006471.2:c.957T>A	XP_016861960.1:p.Pro319=
XM_024453532.1:c.4587T>A	XP_024309300.1:p.Pro1529=
XM_024453533.1:c.4557T>A	XP_024309301.1:p.Pro1519=
XM_024453534.1:c.4380T>A	XP_024309302.1:p.Pro1460=
XM_024453535.1:c.4350T>A	XP_024309303.1:p.Pro1450=
XM_024453536.1:c.4557T>A	XP_024309304.1:p.Pro1519=
XM_024453537.1:c.4557T>A	XP_024309305.1:p.Pro1519=
NM_001321309.2:c.4029T>A	NP_001308238.1:p.Pro1343=
NM_053025.4:c.4557T>A MANE Select	NP_444253.3:p.Pro1519=
NM_053026.4:c.4350T>A	NP_444254.3:p.Pro1450=
NM_053027.4:c.4557T>A	NP_444255.3:p.Pro1519=
NM_053028.4:c.4350T>A	NP_444256.3:p.Pro1450=