Canonical Allele Identifier: CA212522121

Gene: CRTAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97995216A>C , CM000672.2:g.97995216A>C	GRCh38
NC_000010.10:g.99754973A>C , CM000672.1:g.99754973A>C	GRCh37
NC_000010.9:g.99744963A>C	NCBI36
NG_029831.1:g.40613T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370597.8:c.224+15922T>G MANE Select	ENSP00000359629.3:n.224+15922T>G
ENST00000309155.3:c.200+15922T>G	ENSP00000310810.3:n.200+15922T>G
ENST00000370591.6:c.224+15922T>G	ENSP00000359623.2:n.224+15922T>G
ENST00000370597.7:c.224+15922T>G	ENSP00000359629.3:n.224+15922T>G
NM_001206528.2:c.224+15922T>G	NP_001193457.1:n.224+15922T>G
NM_018058.6:c.224+15922T>G	NP_060528.3:n.224+15922T>G
XM_005269938.3:c.224+15922T>G	XP_005269995.1:n.224+15922T>G
XM_011539917.1:c.224+15922T>G	XP_011538219.1:n.224+15922T>G
XM_005269938.4:c.224+15922T>G	XP_005269995.1:n.224+15922T>G
XM_017016366.1:c.224+15922T>G	XP_016871855.1:n.224+15922T>G
XM_017016367.1:c.224+15922T>G	XP_016871856.1:n.224+15922T>G
NM_018058.7:c.224+15922T>G MANE Select	NP_060528.3:n.224+15922T>G
NM_001206528.3:c.224+15922T>G	NP_001193457.1:n.224+15922T>G