Canonical Allele Identifier: CA2499217214
Gene: GRXCR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1201674
ClinVar RCV Id: RCV001567112
dbSNP Id: rs2109775005
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962984_42962985delinsAG , CM000666.2:g.42962984_42962985delinsAG GRCh38
NC_000004.11:g.42965001_42965002delinsAG , CM000666.1:g.42965001_42965002delinsAG GRCh37
NC_000004.10:g.42659758_42659759delinsAG NCBI36
NG_027718.1:g.74719_74720delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.477_478delinsAG MANE Select ENSP00000382670.2:p.Arg160Gly
ENST00000399770.2:c.477_478delinsAG ENSP00000382670.2:p.Arg160Gly
NM_001080476.2:c.477_478delinsAG NP_001073945.1:p.Arg160Gly
XM_011513691.1:c.114_115delinsAG XP_011511993.1:p.Arg39Gly
NM_001080476.3:c.477_478delinsAG MANE Select NP_001073945.1:p.Arg160Gly
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