Canonical Allele Identifier: CA1930623833

Gene: CRTAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97877733_97877734delinsCA , CM000672.2:g.97877733_97877734delinsCA	GRCh38
NC_000010.10:g.99637490_99637491delinsCA , CM000672.1:g.99637490_99637491delinsCA	GRCh37
NC_000010.9:g.99627480_99627481delinsCA	NCBI36
NG_029831.1:g.158095_158096delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370597.8:c.1819+2515_1819+2516delinsTG MANE Select	ENSP00000359629.3:n.1819+2515_1819+2516delinsTG
ENST00000370597.7:c.1819+2515_1819+2516delinsTG	ENSP00000359629.3:n.1819+2515_1819+2516delinsTG
ENST00000413387.5:c.1464+2515_1464+2516delinsTG	ENSP00000408445.1:n.1464+2515_1464+2516delinsTG
NM_018058.6:c.1819+2515_1819+2516delinsTG	NP_060528.3:n.1819+2515_1819+2516delinsTG
XM_011539917.1:c.1819+2515_1819+2516delinsTG	XP_011538219.1:n.1819+2515_1819+2516delinsTG
XM_017016366.1:c.1819+2515_1819+2516delinsTG	XP_016871855.1:n.1819+2515_1819+2516delinsTG
XM_017016367.1:c.1819+2515_1819+2516delinsTG	XP_016871856.1:n.1819+2515_1819+2516delinsTG
NM_018058.7:c.1819+2515_1819+2516delinsTG MANE Select	NP_060528.3:n.1819+2515_1819+2516delinsTG