Canonical Allele Identifier: CA649636274
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719676_71719677insG , CM000667.2:g.71719676_71719677insG GRCh38
NC_000005.9:g.71015503_71015504insG , CM000667.1:g.71015503_71015504insG GRCh37
NC_000005.8:g.71051259_71051260insG NCBI36
NG_015988.1:g.5514_5515insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.160-204_160-203insG MANE Select ENSP00000296777.4:n.160-204_160-203insG
ENST00000296777.4:c.160-204_160-203insG ENSP00000296777.4:n.160-204_160-203insG
ENST00000513096.1:n.98_99insG
NM_004291.3:c.160-204_160-203insG NP_004282.1:n.160-204_160-203insG
NM_004291.4:c.160-204_160-203insG MANE Select NP_004282.1:n.160-204_160-203insG