Canonical Allele Identifier: CA1554416600
Gene: CARTPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719401A= , CM000667.2:g.71719401A= GRCh38
NC_000005.9:g.71015228A= , CM000667.1:g.71015228A= GRCh37
NC_000005.8:g.71050984A= NCBI36
NG_015988.1:g.5239A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.108A= MANE Select ENSP00000296777.4:p.Arg36=
ENST00000296777.4:c.108A= ENSP00000296777.4:p.Arg36=
NM_004291.3:c.108A= NP_004282.1:p.Arg36=
NM_004291.4:c.108A= MANE Select NP_004282.1:p.Arg36=