Canonical Allele Identifier: CA1554416239
Gene: CARTPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719241C= , CM000667.2:g.71719241C= GRCh38
NC_000005.9:g.71015068C= , CM000667.1:g.71015068C= GRCh37
NC_000005.8:g.71050824C= NCBI36
NG_015988.1:g.5079C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.4:c.-53C= ENSP00000296777.4:n.-53C=
NM_004291.3:c.-53C= NP_004282.1:n.-53C=