Canonical Allele Identifier: CA2442509629

Gene: CHM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.86047532T= , CM000685.2:g.86047532T=	GRCh38
NC_000023.10:g.85302536T= , CM000685.1:g.85302536T=	GRCh37
NC_000023.9:g.85189192T=	NCBI36
NG_009874.2:g.5031A= , LRG_699:g.5031A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000390.4:c.1A= MANE Select	NP_000381.1:p.Met1=
ENST00000357749.7:c.1A= MANE Select	ENSP00000350386.2:p.Met1=
NM_000390.2:c.1A= , LRG_699t1:c.1A=	NP_000381.1:p.Met1=
NM_000390.3:c.1A=	NP_000381.1:p.Met1=
NM_001145414.2:c.1A= , LRG_699t2:c.1A=	NP_001138886.1:p.Met1=
NM_001145414.3:c.1A=	NP_001138886.1:p.Met1=
NM_001145414.4:c.1A=	NP_001138886.1:p.Met1=
ENST00000357749.6:c.1A=	ENSP00000350386.2:p.Met1=
ENST00000483950.1:n.30A=
ENST00000615443.1:c.1A=	ENSP00000484306.1:p.Met1=
XM_017029242.2:c.1A=	XP_016884731.1:p.Met1=
XM_017029246.1:c.-440A=	XP_016884735.1:n.-440A=