Canonical Allele Identifier: CA1554416762
Gene: CARTPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719474G= , CM000667.2:g.71719474G= GRCh38
NC_000005.9:g.71015301G= , CM000667.1:g.71015301G= GRCh37
NC_000005.8:g.71051057G= NCBI36
NG_015988.1:g.5312G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.159+22G= MANE Select ENSP00000296777.4:n.159+22G=
ENST00000296777.4:c.159+22G= ENSP00000296777.4:n.159+22G=
NM_004291.3:c.159+22G= NP_004282.1:n.159+22G=
NM_004291.4:c.159+22G= MANE Select NP_004282.1:n.159+22G=