Canonical Allele Identifier: CA2442509573

Gene: CHM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.86047410T= , CM000685.2:g.86047410T=	GRCh38
NC_000023.10:g.85302414T= , CM000685.1:g.85302414T=	GRCh37
NC_000023.9:g.85189070T=	NCBI36
NG_009874.2:g.5153A= , LRG_699:g.5153A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000357749.7:c.49+74A= MANE Select	ENSP00000350386.2:n.49+74A=
ENST00000357749.6:c.49+74A=	ENSP00000350386.2:n.49+74A=
ENST00000483950.1:n.78+74A=
ENST00000615443.1:c.49+74A=	ENSP00000484306.1:n.49+74A=
NM_000390.2:c.49+74A= , LRG_699t1:c.49+74A=	NP_000381.1:n.49+74A=
NM_001145414.2:c.49+74A= , LRG_699t2:c.49+74A=	NP_001138886.1:n.49+74A=
NM_000390.3:c.49+74A=	NP_000381.1:n.49+74A=
NM_001145414.3:c.49+74A=	NP_001138886.1:n.49+74A=
XM_017029242.2:c.49+74A=	XP_016884731.1:n.49+74A=
XM_017029246.1:c.-392+74A=	XP_016884735.1:n.-392+74A=
NM_000390.4:c.49+74A= MANE Select	NP_000381.1:n.49+74A=
NM_001145414.4:c.49+74A=	NP_001138886.1:n.49+74A=