Canonical Allele Identifier: CA1554416292
Gene: CARTPT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719275_71719278delinsAACG , CM000667.2:g.71719275_71719278delinsAACG GRCh38
NC_000005.9:g.71015102_71015105delinsAACG , CM000667.1:g.71015102_71015105delinsAACG GRCh37
NC_000005.8:g.71050858_71050861delinsAACG NCBI36
NG_015988.1:g.5113_5116delinsAACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.-19_-16delinsAACG MANE Select ENSP00000296777.4:n.-19_-16delinsAACG
ENST00000296777.4:c.-19_-16delinsAACG ENSP00000296777.4:n.-19_-16delinsAACG
NM_004291.3:c.-19_-16delinsAACG NP_004282.1:n.-19_-16delinsAACG
NM_004291.4:c.-19_-16delinsAACG MANE Select NP_004282.1:n.-19_-16delinsAACG
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