Canonical Allele Identifier: CA2670496482
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963028del , CM000666.2:g.42963028del GRCh38
NC_000004.11:g.42965045del , CM000666.1:g.42965045del GRCh37
NC_000004.10:g.42659802del NCBI36
NG_027718.1:g.74763del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.521del MANE Select ENSP00000382670.2:p.Asn174ThrfsTer2
ENST00000399770.2:c.521del ENSP00000382670.2:p.Asn174ThrfsTer2
NM_001080476.2:c.521del NP_001073945.1:p.Asn174ThrfsTer2
XM_011513691.1:c.158del XP_011511993.1:p.Asn53ThrfsTer2
NM_001080476.3:c.521del MANE Select NP_001073945.1:p.Asn174ThrfsTer2