Canonical Allele Identifier: CA2674169233
Gene: CARTPT HGNC NCBI

Linked Data

gnomAD v4: 5-71719280-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719280C>A , CM000667.2:g.71719280C>A GRCh38
NC_000005.9:g.71015107C>A , CM000667.1:g.71015107C>A GRCh37
NC_000005.8:g.71050863C>A NCBI36
NG_015988.1:g.5118C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.-14C>A MANE Select ENSP00000296777.4:n.-14C>A
ENST00000296777.4:c.-14C>A ENSP00000296777.4:n.-14C>A
NM_004291.3:c.-14C>A NP_004282.1:n.-14C>A
NM_004291.4:c.-14C>A MANE Select NP_004282.1:n.-14C>A
Search 100 bp 5'
Search 100 bp 3'