Canonical Allele Identifier: CA1554417094
Gene: CARTPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719651A= , CM000667.2:g.71719651A= GRCh38
NC_000005.9:g.71015478A= , CM000667.1:g.71015478A= GRCh37
NC_000005.8:g.71051234A= NCBI36
NG_015988.1:g.5489A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.159+199A= MANE Select ENSP00000296777.4:n.159+199A=
ENST00000296777.4:c.159+199A= ENSP00000296777.4:n.159+199A=
ENST00000513096.1:n.73A=
NM_004291.3:c.159+199A= NP_004282.1:n.159+199A=
NM_004291.4:c.159+199A= MANE Select NP_004282.1:n.159+199A=