Canonical Allele Identifier: CA1453073867

Gene: GRXCR1

Linked Data

• dbSNP Id: rs1748166753

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42963161_42963162insCTAACCAG , CM000666.2:g.42963161_42963162insCTAACCAG	GRCh38
NC_000004.11:g.42965178_42965179insCTAACCAG , CM000666.1:g.42965178_42965179insCTAACCAG	GRCh37
NC_000004.10:g.42659935_42659936insCTAACCAG	NCBI36
NG_027718.1:g.74896_74897insCTAACCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.627+27_627+28insCTAACCAG MANE Select	ENSP00000382670.2:n.627+27_627+28insCTAACCAG
ENST00000399770.2:c.627+27_627+28insCTAACCAG	ENSP00000382670.2:n.627+27_627+28insCTAACCAG
NM_001080476.2:c.627+27_627+28insCTAACCAG	NP_001073945.1:n.627+27_627+28insCTAACCAG
XM_011513691.1:c.264+27_264+28insCTAACCAG	XP_011511993.1:n.264+27_264+28insCTAACCAG
NM_001080476.3:c.627+27_627+28insCTAACCAG MANE Select	NP_001073945.1:n.627+27_627+28insCTAACCAG