Canonical Allele Identifier: CA649636252
Gene: CARTPT HGNC NCBI

Linked Data

COSMIC: COSN19691199
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719291dup , CM000667.2:g.71719291dup GRCh38
NC_000005.9:g.71015118dup , CM000667.1:g.71015118dup GRCh37
NC_000005.8:g.71050874dup NCBI36
NG_015988.1:g.5129dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.-3dup MANE Select ENSP00000296777.4:n.-3dup
ENST00000296777.4:c.-3dup ENSP00000296777.4:n.-3dup
NM_004291.3:c.-3dup NP_004282.1:n.-3dup
NM_004291.4:c.-3dup MANE Select NP_004282.1:n.-3dup
Search 100 bp 5'
Search 100 bp 3'