Canonical Allele Identifier: CA2709255091

Gene: CARTPT

Linked Data

• dbSNP Id: rs2112520827

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71719589A>C , CM000667.2:g.71719589A>C	GRCh38
NC_000005.9:g.71015416A>C , CM000667.1:g.71015416A>C	GRCh37
NC_000005.8:g.71051172A>C	NCBI36
NG_015988.1:g.5427A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296777.5:c.159+137A>C MANE Select	ENSP00000296777.4:n.159+137A>C
ENST00000296777.4:c.159+137A>C	ENSP00000296777.4:n.159+137A>C
ENST00000513096.1:n.11A>C
NM_004291.3:c.159+137A>C	NP_004282.1:n.159+137A>C
NM_004291.4:c.159+137A>C MANE Select	NP_004282.1:n.159+137A>C