Canonical Allele Identifier: CA1930623872

Gene: CRTAC1

Linked Data

• dbSNP Id: rs2050164450

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97877759C>A , CM000672.2:g.97877759C>A	GRCh38
NC_000010.10:g.99637516C>A , CM000672.1:g.99637516C>A	GRCh37
NC_000010.9:g.99627506C>A	NCBI36
NG_029831.1:g.158070G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370597.8:c.1819+2490G>T MANE Select	ENSP00000359629.3:n.1819+2490G>T
ENST00000370597.7:c.1819+2490G>T	ENSP00000359629.3:n.1819+2490G>T
ENST00000413387.5:c.1464+2490G>T	ENSP00000408445.1:n.1464+2490G>T
NM_018058.6:c.1819+2490G>T	NP_060528.3:n.1819+2490G>T
XM_011539917.1:c.1819+2490G>T	XP_011538219.1:n.1819+2490G>T
XM_017016366.1:c.1819+2490G>T	XP_016871855.1:n.1819+2490G>T
XM_017016367.1:c.1819+2490G>T	XP_016871856.1:n.1819+2490G>T
NM_018058.7:c.1819+2490G>T MANE Select	NP_060528.3:n.1819+2490G>T