Canonical Allele Identifier: CA2442480622

Gene: CHM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85963926G= , CM000685.2:g.85963926G=	GRCh38
NC_000023.10:g.85218931G= , CM000685.1:g.85218931G=	GRCh37
NC_000023.9:g.85105587G=	NCBI36
NG_009874.2:g.88637C= , LRG_699:g.88637C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357749.7:c.441C= MANE Select	ENSP00000350386.2:p.Ser147=
ENST00000357749.6:c.441C=	ENSP00000350386.2:p.Ser147=
ENST00000467744.2:n.126+63565C=
NM_000390.2:c.441C= , LRG_699t1:c.441C=	NP_000381.1:p.Ser147=
XM_006724615.2:c.378C=	XP_006724678.1:p.Ser126=
XM_011530839.1:c.-4C=	XP_011529141.1:n.-4C=
NM_000390.3:c.441C=	NP_000381.1:p.Ser147=
NM_001320959.1:c.-4C=	NP_001307888.1:n.-4C=
NM_001362517.1:c.-4C=	NP_001349446.1:n.-4C=
NM_001362518.1:c.-4C=	NP_001349447.1:n.-4C=
NM_001362519.1:c.-4C=	NP_001349448.1:n.-4C=
XM_017029242.2:c.441C=	XP_016884731.1:p.Ser147=
XM_017029246.1:c.-4C=	XP_016884735.1:n.-4C=
XM_024452331.1:c.-4C=	XP_024308099.1:n.-4C=
NM_000390.4:c.441C= MANE Select	NP_000381.1:p.Ser147=
NM_001362518.2:c.-4C=	NP_001349447.1:n.-4C=