Canonical Allele Identifier: CA1554416299
Gene: CARTPT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719277C= , CM000667.2:g.71719277C= GRCh38
NC_000005.9:g.71015104C= , CM000667.1:g.71015104C= GRCh37
NC_000005.8:g.71050860C= NCBI36
NG_015988.1:g.5115C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.-17C= MANE Select ENSP00000296777.4:n.-17C=
ENST00000296777.4:c.-17C= ENSP00000296777.4:n.-17C=
NM_004291.3:c.-17C= NP_004282.1:n.-17C=
NM_004291.4:c.-17C= MANE Select NP_004282.1:n.-17C=
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