Canonical Allele Identifier: CA360104249
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719333G>C , CM000667.2:g.71719333G>C GRCh38
NC_000005.9:g.71015160G>C , CM000667.1:g.71015160G>C GRCh37
NC_000005.8:g.71050916G>C NCBI36
NG_015988.1:g.5171G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.40G>C MANE Select ENSP00000296777.4:p.Ala14Pro
ENST00000296777.4:c.40G>C ENSP00000296777.4:p.Ala14Pro
NM_004291.3:c.40G>C NP_004282.1:p.Ala14Pro
NM_004291.4:c.40G>C MANE Select NP_004282.1:p.Ala14Pro