Canonical Allele Identifier: CA1554417053
Gene: CARTPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719625C= , CM000667.2:g.71719625C= GRCh38
NC_000005.9:g.71015452C= , CM000667.1:g.71015452C= GRCh37
NC_000005.8:g.71051208C= NCBI36
NG_015988.1:g.5463C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.159+173C= MANE Select ENSP00000296777.4:n.159+173C=
ENST00000296777.4:c.159+173C= ENSP00000296777.4:n.159+173C=
ENST00000513096.1:n.47C=
NM_004291.3:c.159+173C= NP_004282.1:n.159+173C=
NM_004291.4:c.159+173C= MANE Select NP_004282.1:n.159+173C=