Canonical Allele Identifier: CA360104472
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719442A>T , CM000667.2:g.71719442A>T GRCh38
NC_000005.9:g.71015269A>T , CM000667.1:g.71015269A>T GRCh37
NC_000005.8:g.71051025A>T NCBI36
NG_015988.1:g.5280A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.149A>T MANE Select ENSP00000296777.4:p.Glu50Val
ENST00000296777.4:c.149A>T ENSP00000296777.4:p.Glu50Val
NM_004291.3:c.149A>T NP_004282.1:p.Glu50Val
NM_004291.4:c.149A>T MANE Select NP_004282.1:p.Glu50Val