Canonical Allele Identifier: CA2403809700

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36312438G= , CM000684.2:g.36312438G=	GRCh38
NC_000022.10:g.36708483G= , CM000684.1:g.36708483G=	GRCh37
NC_000022.9:g.35038429G=	NCBI36
NG_011884.2:g.80581C= , LRG_567:g.80581C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.1555-216C= MANE Select	NP_002464.1:n.1555-216C=
ENST00000216181.11:c.1555-216C= MANE Select	ENSP00000216181.6:n.1555-216C=
NM_002473.5:c.1555-216C= , LRG_567t1:c.1555-216C=	NP_002464.1:n.1555-216C=
ENST00000216181.9:c.1555-216C=	ENSP00000216181.5:n.1555-216C=
ENST00000685187.1:n.1769-216C=
ENST00000685801.1:c.1555-216C=	ENSP00000510688.1:n.1555-216C=
ENST00000691109.1:n.1850-216C=
ENST00000691687.1:n.2353-216C=
ENST00000692930.1:n.1769-216C=
XM_011530197.1:c.1555-216C=	XP_011528499.1:n.1555-216C=
XM_011530197.2:c.1555-216C=	XP_011528499.1:n.1555-216C=
XM_017028803.1:c.1555-216C=	XP_016884292.1:n.1555-216C=
XM_017028804.1:c.1555-216C=	XP_016884293.1:n.1555-216C=
XM_017028805.1:c.1555-216C=	XP_016884294.1:n.1555-216C=
XM_017028806.1:c.1555-216C=	XP_016884295.1:n.1555-216C=