Canonical Allele Identifier: CA2670496509
Gene: GRXCR1 HGNC NCBI

Linked Data

gnomAD v4: 4-42963175-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963177del , CM000666.2:g.42963177del GRCh38
NC_000004.11:g.42965194del , CM000666.1:g.42965194del GRCh37
NC_000004.10:g.42659951del NCBI36
NG_027718.1:g.74912del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+43del MANE Select ENSP00000382670.2:n.627+43del
ENST00000399770.2:c.627+43del ENSP00000382670.2:n.627+43del
NM_001080476.2:c.627+43del NP_001073945.1:n.627+43del
XM_011513691.1:c.264+43del XP_011511993.1:n.264+43del
NM_001080476.3:c.627+43del MANE Select NP_001073945.1:n.627+43del
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