Canonical Allele Identifier: CA413787104

Gene: CHM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85963898G>A , CM000685.2:g.85963898G>A	GRCh38
NC_000023.10:g.85218903G>A , CM000685.1:g.85218903G>A	GRCh37
NC_000023.9:g.85105559G>A	NCBI36
NG_009874.2:g.88665C>T , LRG_699:g.88665C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000390.4:c.469C>T MANE Select	NP_000381.1:p.Gln157Ter
ENST00000357749.7:c.469C>T MANE Select	ENSP00000350386.2:p.Gln157Ter
NM_000390.2:c.469C>T , LRG_699t1:c.469C>T	NP_000381.1:p.Gln157Ter
NM_000390.3:c.469C>T	NP_000381.1:p.Gln157Ter
NM_001320959.1:c.25C>T	NP_001307888.1:p.Gln9Ter
NM_001362517.1:c.25C>T	NP_001349446.1:p.Gln9Ter
NM_001362518.1:c.25C>T	NP_001349447.1:p.Gln9Ter
NM_001362518.2:c.25C>T	NP_001349447.1:p.Gln9Ter
NM_001362519.1:c.25C>T	NP_001349448.1:p.Gln9Ter
ENST00000357749.6:c.469C>T	ENSP00000350386.2:p.Gln157Ter
ENST00000467744.2:n.126+63593C>T
XM_006724615.2:c.406C>T	XP_006724678.1:p.Gln136Ter
XM_011530839.1:c.25C>T	XP_011529141.1:p.Gln9Ter
XM_017029242.2:c.469C>T	XP_016884731.1:p.Gln157Ter
XM_017029246.1:c.25C>T	XP_016884735.1:p.Gln9Ter
XM_024452331.1:c.25C>T	XP_024308099.1:p.Gln9Ter