Canonical Allele Identifier: CA2442478046

Gene: CHM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85956305C= , CM000685.2:g.85956305C=	GRCh38
NC_000023.10:g.85211310C= , CM000685.1:g.85211310C=	GRCh37
NC_000023.9:g.85097966C=	NCBI36
NG_009874.2:g.96258G= , LRG_699:g.96258G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000357749.7:c.1014G= MANE Select	ENSP00000350386.2:p.Met338=
ENST00000357749.6:c.1014G=	ENSP00000350386.2:p.Met338=
ENST00000467744.2:n.126+71186G=
NM_000390.2:c.1014G= , LRG_699t1:c.1014G=	NP_000381.1:p.Met338=
XM_006724615.2:c.951G=	XP_006724678.1:p.Met317=
XM_011530839.1:c.570G=	XP_011529141.1:p.Met190=
NM_000390.3:c.1014G=	NP_000381.1:p.Met338=
NM_001320959.1:c.570G=	NP_001307888.1:p.Met190=
NM_001362517.1:c.570G=	NP_001349446.1:p.Met190=
NM_001362518.1:c.570G=	NP_001349447.1:p.Met190=
NM_001362519.1:c.570G=	NP_001349448.1:p.Met190=
XM_017029242.2:c.1014G=	XP_016884731.1:p.Met338=
XM_017029246.1:c.570G=	XP_016884735.1:p.Met190=
XM_024452331.1:c.570G=	XP_024308099.1:p.Met190=
NM_000390.4:c.1014G= MANE Select	NP_000381.1:p.Met338=
NM_001362518.2:c.570G=	NP_001349447.1:p.Met190=