Canonical Allele Identifier: CA360104231

Gene: CARTPT

Linked Data

• MyVariant Identifiers: chr5:g.71015149C>G (hg19) ; chr5:g.71719322C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71719322C>G , CM000667.2:g.71719322C>G	GRCh38
NC_000005.9:g.71015149C>G , CM000667.1:g.71015149C>G	GRCh37
NC_000005.8:g.71050905C>G	NCBI36
NG_015988.1:g.5160C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296777.5:c.29C>G MANE Select	ENSP00000296777.4:p.Pro10Arg
ENST00000296777.4:c.29C>G	ENSP00000296777.4:p.Pro10Arg
NM_004291.3:c.29C>G	NP_004282.1:p.Pro10Arg
NM_004291.4:c.29C>G MANE Select	NP_004282.1:p.Pro10Arg