Canonical Allele Identifier: CA2674169464
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719676_71719677insGCGGCTCAGGGG , CM000667.2:g.71719676_71719677insGCGGCTCAGGGG GRCh38
NC_000005.9:g.71015503_71015504insGCGGCTCAGGGG , CM000667.1:g.71015503_71015504insGCGGCTCAGGGG GRCh37
NC_000005.8:g.71051259_71051260insGCGGCTCAGGGG NCBI36
NG_015988.1:g.5514_5515insGCGGCTCAGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.160-204_160-203insGCGGCTCAGGGG MANE Select ENSP00000296777.4:n.160-204_160-203insGCGGCTCAGGGG
ENST00000296777.4:c.160-204_160-203insGCGGCTCAGGGG ENSP00000296777.4:n.160-204_160-203insGCGGCTCAGGGG
ENST00000513096.1:n.98_99insGCGGCTCAGGGG
NM_004291.3:c.160-204_160-203insGCGGCTCAGGGG NP_004282.1:n.160-204_160-203insGCGGCTCAGGGG
NM_004291.4:c.160-204_160-203insGCGGCTCAGGGG MANE Select NP_004282.1:n.160-204_160-203insGCGGCTCAGGGG