Canonical Allele Identifier: CA360104419
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719417T>G , CM000667.2:g.71719417T>G GRCh38
NC_000005.9:g.71015244T>G , CM000667.1:g.71015244T>G GRCh37
NC_000005.8:g.71051000T>G NCBI36
NG_015988.1:g.5255T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.124T>G MANE Select ENSP00000296777.4:p.Ser42Ala
ENST00000296777.4:c.124T>G ENSP00000296777.4:p.Ser42Ala
NM_004291.3:c.124T>G NP_004282.1:p.Ser42Ala
NM_004291.4:c.124T>G MANE Select NP_004282.1:p.Ser42Ala