Canonical Allele Identifier: CA360104269

Gene: CARTPT

Linked Data

• MyVariant Identifiers: chr5:g.71015172C>A (hg19) ; chr5:g.71719345C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71719345C>A , CM000667.2:g.71719345C>A	GRCh38
NC_000005.9:g.71015172C>A , CM000667.1:g.71015172C>A	GRCh37
NC_000005.8:g.71050928C>A	NCBI36
NG_015988.1:g.5183C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296777.5:c.52C>A MANE Select	ENSP00000296777.4:p.Leu18Met
ENST00000296777.4:c.52C>A	ENSP00000296777.4:p.Leu18Met
NM_004291.3:c.52C>A	NP_004282.1:p.Leu18Met
NM_004291.4:c.52C>A MANE Select	NP_004282.1:p.Leu18Met