Canonical Allele Identifier: CA1554416355
Gene: CARTPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719313G= , CM000667.2:g.71719313G= GRCh38
NC_000005.9:g.71015140G= , CM000667.1:g.71015140G= GRCh37
NC_000005.8:g.71050896G= NCBI36
NG_015988.1:g.5151G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.20G= MANE Select ENSP00000296777.4:p.Arg7=
ENST00000296777.4:c.20G= ENSP00000296777.4:p.Arg7=
NM_004291.3:c.20G= NP_004282.1:p.Arg7=
NM_004291.4:c.20G= MANE Select NP_004282.1:p.Arg7=