Canonical Allele Identifier: CA360104479
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719445A>G , CM000667.2:g.71719445A>G GRCh38
NC_000005.9:g.71015272A>G , CM000667.1:g.71015272A>G GRCh37
NC_000005.8:g.71051028A>G NCBI36
NG_015988.1:g.5283A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.152A>G MANE Select ENSP00000296777.4:p.Lys51Arg
ENST00000296777.4:c.152A>G ENSP00000296777.4:p.Lys51Arg
NM_004291.3:c.152A>G NP_004282.1:p.Lys51Arg
NM_004291.4:c.152A>G MANE Select NP_004282.1:p.Lys51Arg