Canonical Allele Identifier: CA2442486887
Gene: CHM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.85981804C= , CM000685.2:g.85981804C= GRCh38
NC_000023.10:g.85236808C= , CM000685.1:g.85236808C= GRCh37
NC_000023.9:g.85123464C= NCBI36
NG_009874.2:g.70759G= , LRG_699:g.70759G=

Transcript Alleles

HGVS Amino-acid change
ENST00000357749.7:c.122G= MANE Select ENSP00000350386.2:p.Ser41=
ENST00000357749.6:c.122G= ENSP00000350386.2:p.Ser41=
ENST00000467744.2:n.126+45687G=
ENST00000487515.1:n.6G=
ENST00000615443.1:c.122G= ENSP00000484306.1:p.Ser41=
NM_000390.2:c.122G= , LRG_699t1:c.122G= NP_000381.1:p.Ser41=
NM_001145414.2:c.122G= , LRG_699t2:c.122G= NP_001138886.1:p.Ser41=
XM_006724615.2:c.59G= XP_006724678.1:p.Ser20=
XM_011530839.1:c.-323G= XP_011529141.1:n.-323G=
NM_000390.3:c.122G= NP_000381.1:p.Ser41=
NM_001145414.3:c.122G= NP_001138886.1:p.Ser41=
NM_001320959.1:c.-323G= NP_001307888.1:n.-323G=
NM_001362517.1:c.-323G= NP_001349446.1:n.-323G=
NM_001362518.1:c.-319G= NP_001349447.1:n.-319G=
NM_001362519.1:c.-319G= NP_001349448.1:n.-319G=
XM_017029242.2:c.122G= XP_016884731.1:p.Ser41=
XM_017029246.1:c.-319G= XP_016884735.1:n.-319G=
XM_024452331.1:c.-323G= XP_024308099.1:n.-323G=
NM_000390.4:c.122G= MANE Select NP_000381.1:p.Ser41=
NM_001145414.4:c.122G= NP_001138886.1:p.Ser41=
NM_001362518.2:c.-319G= NP_001349447.1:n.-319G=