Canonical Allele Identifier: CA1554416306
Gene: CARTPT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719279A= , CM000667.2:g.71719279A= GRCh38
NC_000005.9:g.71015106A= , CM000667.1:g.71015106A= GRCh37
NC_000005.8:g.71050862A= NCBI36
NG_015988.1:g.5117A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.-15A= MANE Select ENSP00000296777.4:n.-15A=
ENST00000296777.4:c.-15A= ENSP00000296777.4:n.-15A=
NM_004291.3:c.-15A= NP_004282.1:n.-15A=
NM_004291.4:c.-15A= MANE Select NP_004282.1:n.-15A=
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