Canonical Allele Identifier: CA2832547347
Gene: CARTPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719480dup , CM000667.2:g.71719480dup GRCh38
NC_000005.9:g.71015307dup , CM000667.1:g.71015307dup GRCh37
NC_000005.8:g.71051063dup NCBI36
NG_015988.1:g.5318dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.159+28dup MANE Select ENSP00000296777.4:n.159+28dup
ENST00000296777.4:c.159+28dup ENSP00000296777.4:n.159+28dup
NM_004291.3:c.159+28dup NP_004282.1:n.159+28dup
NM_004291.4:c.159+28dup MANE Select NP_004282.1:n.159+28dup