Canonical Allele Identifier: CA360104190
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719301G>C , CM000667.2:g.71719301G>C GRCh38
NC_000005.9:g.71015128G>C , CM000667.1:g.71015128G>C GRCh37
NC_000005.8:g.71050884G>C NCBI36
NG_015988.1:g.5139G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.8G>C MANE Select ENSP00000296777.4:p.Ser3Thr
ENST00000296777.4:c.8G>C ENSP00000296777.4:p.Ser3Thr
NM_004291.3:c.8G>C NP_004282.1:p.Ser3Thr
NM_004291.4:c.8G>C MANE Select NP_004282.1:p.Ser3Thr