Canonical Allele Identifier: CA1554416528
Gene: CARTPT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719374C= , CM000667.2:g.71719374C= GRCh38
NC_000005.9:g.71015201C= , CM000667.1:g.71015201C= GRCh37
NC_000005.8:g.71050957C= NCBI36
NG_015988.1:g.5212C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.81C= MANE Select ENSP00000296777.4:p.Ala27=
ENST00000296777.4:c.81C= ENSP00000296777.4:p.Ala27=
NM_004291.3:c.81C= NP_004282.1:p.Ala27=
NM_004291.4:c.81C= MANE Select NP_004282.1:p.Ala27=
Search 100 bp 5'
Search 100 bp 3'