Canonical Allele Identifier: CA10209676

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36295537C>T , CM000684.2:g.36295537C>T	GRCh38
NC_000022.10:g.36691583C>T , CM000684.1:g.36691583C>T	GRCh37
NC_000022.9:g.35021529C>T	NCBI36
NG_011884.2:g.97482G>A , LRG_567:g.97482G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.3453G>A MANE Select	NP_002464.1:p.Thr1151=
ENST00000216181.11:c.3453G>A MANE Select	ENSP00000216181.6:p.Thr1151=
NM_002473.5:c.3453G>A , LRG_567t1:c.3453G>A	NP_002464.1:p.Thr1151=
ENST00000216181.9:c.3453G>A	ENSP00000216181.5:p.Thr1151=
ENST00000459960.1:n.662G>A
ENST00000685801.1:c.3516G>A	ENSP00000510688.1:p.Thr1172=
ENST00000691109.1:n.3748G>A
XM_011530197.1:c.3453G>A	XP_011528499.1:p.Thr1151=
XM_011530197.2:c.3453G>A	XP_011528499.1:p.Thr1151=
XM_017028803.1:c.3453G>A	XP_016884292.1:p.Thr1151=
XM_017028804.1:c.3453G>A	XP_016884293.1:p.Thr1151=
XM_017028805.1:c.3453G>A	XP_016884294.1:p.Thr1151=
XM_017028806.1:c.3453G>A	XP_016884295.1:p.Thr1151=