Canonical Allele Identifier: CA2840872622

Gene: MYH11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15750097C>A , CM000678.2:g.15750097C>A	GRCh38
NC_000016.9:g.15843954C>A , CM000678.1:g.15843954C>A	GRCh37
NC_000016.8:g.15751455C>A	NCBI36
NG_009299.1:g.111934G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300036.6:c.2058+41G>T MANE Select	ENSP00000300036.5:n.2058+41G>T
ENST00000452625.7:c.2079+41G>T MANE Plus Clinical	ENSP00000407821.2:n.2079+41G>T
ENST00000576790.7:c.2058+41G>T	ENSP00000458731.1:n.2058+41G>T
ENST00000652121.1:c.*241+41G>T	ENSP00000498314.1:n.*241+41G>T
ENST00000300036.5:c.2058+41G>T	ENSP00000300036.5:n.2058+41G>T
ENST00000396324.7:c.2079+41G>T	ENSP00000379616.3:n.2079+41G>T
ENST00000452625.6:c.2079+41G>T	ENSP00000407821.2:n.2079+41G>T
ENST00000570785.1:n.2521G>T
ENST00000576790.6:c.2058+41G>T	ENSP00000458731.1:n.2058+41G>T
ENST00000616439.4:c.2079+41G>T	ENSP00000484924.1:n.2079+41G>T
NM_001040113.1:c.2079+41G>T	NP_001035202.1:n.2079+41G>T
NM_001040114.1:c.2079+41G>T	NP_001035203.1:n.2079+41G>T
NM_002474.2:c.2058+41G>T	NP_002465.1:n.2058+41G>T
NM_022844.2:c.2058+41G>T	NP_074035.1:n.2058+41G>T
XM_011522502.1:c.2058+41G>T	XP_011520804.1:n.2058+41G>T
XM_011522502.2:c.2058+41G>T	XP_011520804.1:n.2058+41G>T
XM_017023250.1:c.2079+41G>T	XP_016878739.1:n.2079+41G>T
NM_002474.3:c.2058+41G>T MANE Select	NP_002465.1:n.2058+41G>T
NM_001040113.2:c.2079+41G>T MANE Plus Clinical	NP_001035202.1:n.2079+41G>T
NM_001040114.2:c.2079+41G>T	NP_001035203.1:n.2079+41G>T
NM_022844.3:c.2058+41G>T	NP_074035.1:n.2058+41G>T