Canonical Allele Identifier: CA7922585

Gene: MYH11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15757820C>T , CM000678.2:g.15757820C>T	GRCh38
NC_000016.9:g.15851677C>T , CM000678.1:g.15851677C>T	GRCh37
NC_000016.8:g.15759178C>T	NCBI36
NG_009299.1:g.104211G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300036.6:c.1575+7G>A MANE Select	ENSP00000300036.5:n.1575+7G>A
ENST00000452625.7:c.1596+7G>A MANE Plus Clinical	ENSP00000407821.2:n.1596+7G>A
ENST00000576790.7:c.1575+7G>A	ENSP00000458731.1:n.1575+7G>A
ENST00000652121.1:c.1575+7G>A	ENSP00000498314.1:n.1575+7G>A
ENST00000300036.5:c.1575+7G>A	ENSP00000300036.5:n.1575+7G>A
ENST00000396324.7:c.1596+7G>A	ENSP00000379616.3:n.1596+7G>A
ENST00000452625.6:c.1596+7G>A	ENSP00000407821.2:n.1596+7G>A
ENST00000570785.1:n.1997+7G>A
ENST00000576790.6:c.1575+7G>A	ENSP00000458731.1:n.1575+7G>A
ENST00000616439.4:c.1596+7G>A	ENSP00000484924.1:n.1596+7G>A
NM_001040113.1:c.1596+7G>A	NP_001035202.1:n.1596+7G>A
NM_001040114.1:c.1596+7G>A	NP_001035203.1:n.1596+7G>A
NM_002474.2:c.1575+7G>A	NP_002465.1:n.1575+7G>A
NM_022844.2:c.1575+7G>A	NP_074035.1:n.1575+7G>A
XM_011522502.1:c.1575+7G>A	XP_011520804.1:n.1575+7G>A
XM_011522502.2:c.1575+7G>A	XP_011520804.1:n.1575+7G>A
XM_017023250.1:c.1596+7G>A	XP_016878739.1:n.1596+7G>A
NM_002474.3:c.1575+7G>A MANE Select	NP_002465.1:n.1575+7G>A
NM_001040113.2:c.1596+7G>A MANE Plus Clinical	NP_001035202.1:n.1596+7G>A
NM_001040114.2:c.1596+7G>A	NP_001035203.1:n.1596+7G>A
NM_022844.3:c.1575+7G>A	NP_074035.1:n.1575+7G>A