Canonical Allele Identifier: CA2580068662

Gene: MYLK

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123733989_123733991delinsAGA , CM000665.2:g.123733989_123733991delinsAGA	GRCh38
NC_000003.11:g.123452836_123452838delinsAGA , CM000665.1:g.123452836_123452838delinsAGA	GRCh37
NC_000003.10:g.124935526_124935528delinsAGA	NCBI36
NG_029111.1:g.155312_155314delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346322.10:c.1005_1007delinsTCT	ENSP00000320622.6:p.Pro336Leu
ENST00000686406.1:c.1005_1007delinsTCT	ENSP00000509044.1:p.Pro336Leu
ENST00000686761.1:c.1005_1007delinsTCT	ENSP00000508758.1:p.Pro336Leu
ENST00000686822.1:n.1106_1108delinsTCT
ENST00000687848.1:c.1035_1037delinsTCT	ENSP00000508761.1:p.Pro346Leu
ENST00000690457.1:c.754+3387_754+3389delinsTCT	ENSP00000508777.1:n.754+3387_754+3389delinsTCT
ENST00000693689.1:c.1005_1007delinsTCT	ENSP00000510503.1:p.Pro336Leu
ENST00000360304.8:c.1005_1007delinsTCT MANE Select	ENSP00000353452.3:p.Pro336Leu
ENST00000346322.9:c.1005_1007delinsTCT	ENSP00000320622.5:p.Pro336Leu
ENST00000354792.9:c.1005_1007delinsTCT	ENSP00000346846.6:p.Pro336Leu
ENST00000359169.5:c.1005_1007delinsTCT	ENSP00000352088.1:p.Pro336Leu
ENST00000360304.7:c.1005_1007delinsTCT	ENSP00000353452.3:p.Pro336Leu
ENST00000360772.7:c.1005_1007delinsTCT	ENSP00000354004.3:p.Pro336Leu
ENST00000464489.5:c.*584_*586delinsTCT	ENSP00000417798.1:n.*584_*586delinsTCT
ENST00000475616.5:c.1005_1007delinsTCT	ENSP00000418335.1:p.Pro336Leu
ENST00000514623.1:n.1780_1782delinsTCT
NM_053025.3:c.1005_1007delinsTCT	NP_444253.3:p.Pro336Leu
NM_053026.3:c.1005_1007delinsTCT	NP_444254.3:p.Pro336Leu
NM_053027.3:c.1005_1007delinsTCT	NP_444255.3:p.Pro336Leu
NM_053028.3:c.1005_1007delinsTCT	NP_444256.3:p.Pro336Leu
XM_011512860.1:c.1005_1007delinsTCT	XP_011511162.1:p.Pro336Leu
XM_011512861.1:c.1005_1007delinsTCT	XP_011511163.1:p.Pro336Leu
XM_011512862.1:c.477_479delinsTCT	XP_011511164.1:p.Pro160Leu
NM_001321309.1:c.477_479delinsTCT	NP_001308238.1:p.Pro160Leu
XM_011512860.3:c.1035_1037delinsTCT	XP_011511162.2:p.Pro346Leu
XM_011512861.3:c.1035_1037delinsTCT	XP_011511163.2:p.Pro346Leu
XM_024453532.1:c.1035_1037delinsTCT	XP_024309300.1:p.Pro346Leu
XM_024453533.1:c.1005_1007delinsTCT	XP_024309301.1:p.Pro336Leu
XM_024453534.1:c.1035_1037delinsTCT	XP_024309302.1:p.Pro346Leu
XM_024453535.1:c.1005_1007delinsTCT	XP_024309303.1:p.Pro336Leu
XM_024453536.1:c.1005_1007delinsTCT	XP_024309304.1:p.Pro336Leu
XM_024453537.1:c.1005_1007delinsTCT	XP_024309305.1:p.Pro336Leu
NM_001321309.2:c.477_479delinsTCT	NP_001308238.1:p.Pro160Leu
NM_053025.4:c.1005_1007delinsTCT MANE Select	NP_444253.3:p.Pro336Leu
NM_053026.4:c.1005_1007delinsTCT	NP_444254.3:p.Pro336Leu
NM_053027.4:c.1005_1007delinsTCT	NP_444255.3:p.Pro336Leu
NM_053028.4:c.1005_1007delinsTCT	NP_444256.3:p.Pro336Leu