Canonical Allele Identifier: CA16620076

Gene: MYH11

Linked Data

• ClinVar Variation Id: 421270
• ClinVar RCV Id: RCV000485034 ; RCV001184325
• dbSNP Id: rs1064795023
• gnomAD v4: 16-15738685-G-A
• COSMIC: COSM4704537 ; COSM4704538
• MyVariant Identifiers: chr16:g.15832542G>A (hg19) ; chr16:g.15738685G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15738685G>A , CM000678.2:g.15738685G>A	GRCh38
NC_000016.9:g.15832542G>A , CM000678.1:g.15832542G>A	GRCh37
NC_000016.8:g.15740043G>A	NCBI36
NG_009299.1:g.123346C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300036.6:c.3001C>T MANE Select	ENSP00000300036.5:p.Arg1001Ter
ENST00000452625.7:c.3022C>T MANE Plus Clinical	ENSP00000407821.2:p.Arg1008Ter
ENST00000576790.7:c.3001C>T	ENSP00000458731.1:p.Arg1001Ter
ENST00000652121.1:c.*1184C>T	ENSP00000498314.1:n.*1184C>T
ENST00000300036.5:c.3001C>T	ENSP00000300036.5:p.Arg1001Ter
ENST00000396324.7:c.3022C>T	ENSP00000379616.3:p.Arg1008Ter
ENST00000452625.6:c.3022C>T	ENSP00000407821.2:p.Arg1008Ter
ENST00000576790.6:c.3001C>T	ENSP00000458731.1:p.Arg1001Ter
ENST00000616439.4:c.3022C>T	ENSP00000484924.1:p.Arg1008Ter
NM_001040113.1:c.3022C>T	NP_001035202.1:p.Arg1008Ter
NM_001040114.1:c.3022C>T	NP_001035203.1:p.Arg1008Ter
NM_002474.2:c.3001C>T	NP_002465.1:p.Arg1001Ter
NM_022844.2:c.3001C>T	NP_074035.1:p.Arg1001Ter
XM_011522502.1:c.3001C>T	XP_011520804.1:p.Arg1001Ter
XM_011522502.2:c.3001C>T	XP_011520804.1:p.Arg1001Ter
XM_017023250.1:c.3022C>T	XP_016878739.1:p.Arg1008Ter
NM_002474.3:c.3001C>T MANE Select	NP_002465.1:p.Arg1001Ter
NM_001040113.2:c.3022C>T MANE Plus Clinical	NP_001035202.1:p.Arg1008Ter
NM_001040114.2:c.3022C>T	NP_001035203.1:p.Arg1008Ter
NM_022844.3:c.3001C>T	NP_074035.1:p.Arg1001Ter