Canonical Allele Identifier: CA1930623863

Gene: CRTAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97877750_97877751delinsCT , CM000672.2:g.97877750_97877751delinsCT	GRCh38
NC_000010.10:g.99637507_99637508delinsCT , CM000672.1:g.99637507_99637508delinsCT	GRCh37
NC_000010.9:g.99627497_99627498delinsCT	NCBI36
NG_029831.1:g.158078_158079delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000370597.8:c.1819+2498_1819+2499delinsAG MANE Select	ENSP00000359629.3:n.1819+2498_1819+2499delinsAG
ENST00000370597.7:c.1819+2498_1819+2499delinsAG	ENSP00000359629.3:n.1819+2498_1819+2499delinsAG
ENST00000413387.5:c.1464+2498_1464+2499delinsAG	ENSP00000408445.1:n.1464+2498_1464+2499delinsAG
NM_018058.6:c.1819+2498_1819+2499delinsAG	NP_060528.3:n.1819+2498_1819+2499delinsAG
XM_011539917.1:c.1819+2498_1819+2499delinsAG	XP_011538219.1:n.1819+2498_1819+2499delinsAG
XM_017016366.1:c.1819+2498_1819+2499delinsAG	XP_016871855.1:n.1819+2498_1819+2499delinsAG
XM_017016367.1:c.1819+2498_1819+2499delinsAG	XP_016871856.1:n.1819+2498_1819+2499delinsAG
NM_018058.7:c.1819+2498_1819+2499delinsAG MANE Select	NP_060528.3:n.1819+2498_1819+2499delinsAG