Canonical Allele Identifier: CA2670496538

Gene: GRXCR1

Linked Data

• gnomAD v4: 4-42963233-CTTGCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42963234_42963238del , CM000666.2:g.42963234_42963238del	GRCh38
NC_000004.11:g.42965251_42965255del , CM000666.1:g.42965251_42965255del	GRCh37
NC_000004.10:g.42660008_42660012del	NCBI36
NG_027718.1:g.74969_74973del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.627+100_627+104del MANE Select	ENSP00000382670.2:n.627+100_627+104del
ENST00000399770.2:c.627+100_627+104del	ENSP00000382670.2:n.627+100_627+104del
NM_001080476.2:c.627+100_627+104del	NP_001073945.1:n.627+100_627+104del
XM_011513691.1:c.264+100_264+104del	XP_011511993.1:n.264+100_264+104del
NM_001080476.3:c.627+100_627+104del MANE Select	NP_001073945.1:n.627+100_627+104del