Canonical Allele Identifier: CA2670496548
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963251del , CM000666.2:g.42963251del GRCh38
NC_000004.11:g.42965268del , CM000666.1:g.42965268del GRCh37
NC_000004.10:g.42660025del NCBI36
NG_027718.1:g.74986del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+117del MANE Select ENSP00000382670.2:n.627+117del
ENST00000399770.2:c.627+117del ENSP00000382670.2:n.627+117del
NM_001080476.2:c.627+117del NP_001073945.1:n.627+117del
XM_011513691.1:c.264+117del XP_011511993.1:n.264+117del
NM_001080476.3:c.627+117del MANE Select NP_001073945.1:n.627+117del