Canonical Allele Identifier: CA2674169457
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719675dup , CM000667.2:g.71719675dup GRCh38
NC_000005.9:g.71015502dup , CM000667.1:g.71015502dup GRCh37
NC_000005.8:g.71051258dup NCBI36
NG_015988.1:g.5513dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.160-205dup MANE Select ENSP00000296777.4:n.160-205dup
ENST00000296777.4:c.160-205dup ENSP00000296777.4:n.160-205dup
ENST00000513096.1:n.97dup
NM_004291.3:c.160-205dup NP_004282.1:n.160-205dup
NM_004291.4:c.160-205dup MANE Select NP_004282.1:n.160-205dup