Canonical Allele Identifier: CA2442480574

Gene: CHM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85963800T= , CM000685.2:g.85963800T=	GRCh38
NC_000023.10:g.85218805T= , CM000685.1:g.85218805T=	GRCh37
NC_000023.9:g.85105461T=	NCBI36
NG_009874.2:g.88763A= , LRG_699:g.88763A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357749.7:c.567A= MANE Select	ENSP00000350386.2:p.Pro189=
ENST00000357749.6:c.567A=	ENSP00000350386.2:p.Pro189=
ENST00000467744.2:n.126+63691A=
NM_000390.2:c.567A= , LRG_699t1:c.567A=	NP_000381.1:p.Pro189=
XM_006724615.2:c.504A=	XP_006724678.1:p.Pro168=
XM_011530839.1:c.123A=	XP_011529141.1:p.Pro41=
NM_000390.3:c.567A=	NP_000381.1:p.Pro189=
NM_001320959.1:c.123A=	NP_001307888.1:p.Pro41=
NM_001362517.1:c.123A=	NP_001349446.1:p.Pro41=
NM_001362518.1:c.123A=	NP_001349447.1:p.Pro41=
NM_001362519.1:c.123A=	NP_001349448.1:p.Pro41=
XM_017029242.2:c.567A=	XP_016884731.1:p.Pro189=
XM_017029246.1:c.123A=	XP_016884735.1:p.Pro41=
XM_024452331.1:c.123A=	XP_024308099.1:p.Pro41=
NM_000390.4:c.567A= MANE Select	NP_000381.1:p.Pro189=
NM_001362518.2:c.123A=	NP_001349447.1:p.Pro41=