Canonical Allele Identifier: CA10465557
Gene: CHM HGNC NCBI

Linked Data

dbSNP Id: rs768528761
gnomAD v2: X-85218758-T-G
gnomAD v4: X-85963753-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.85963753T>G , CM000685.2:g.85963753T>G GRCh38
NC_000023.10:g.85218758T>G , CM000685.1:g.85218758T>G GRCh37
NC_000023.9:g.85105414T>G NCBI36
NG_009874.2:g.88810A>C , LRG_699:g.88810A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357749.7:c.614A>C MANE Select ENSP00000350386.2:p.Asp205Ala
ENST00000357749.6:c.614A>C ENSP00000350386.2:p.Asp205Ala
ENST00000467744.2:n.126+63738A>C
NM_000390.2:c.614A>C , LRG_699t1:c.614A>C NP_000381.1:p.Asp205Ala
XM_006724615.2:c.551A>C XP_006724678.1:p.Asp184Ala
XM_011530839.1:c.170A>C XP_011529141.1:p.Asp57Ala
NM_000390.3:c.614A>C NP_000381.1:p.Asp205Ala
NM_001320959.1:c.170A>C NP_001307888.1:p.Asp57Ala
NM_001362517.1:c.170A>C NP_001349446.1:p.Asp57Ala
NM_001362518.1:c.170A>C NP_001349447.1:p.Asp57Ala
NM_001362519.1:c.170A>C NP_001349448.1:p.Asp57Ala
XM_017029242.2:c.614A>C XP_016884731.1:p.Asp205Ala
XM_017029246.1:c.170A>C XP_016884735.1:p.Asp57Ala
XM_024452331.1:c.170A>C XP_024308099.1:p.Asp57Ala
NM_000390.4:c.614A>C MANE Select NP_000381.1:p.Asp205Ala
NM_001362518.2:c.170A>C NP_001349447.1:p.Asp57Ala