Canonical Allele Identifier: CA2548640030
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963283_42963284insATCAGCCCTGGTTGG , CM000666.2:g.42963283_42963284insATCAGCCCTGGTTGG GRCh38
NC_000004.11:g.42965300_42965301insATCAGCCCTGGTTGG , CM000666.1:g.42965300_42965301insATCAGCCCTGGTTGG GRCh37
NC_000004.10:g.42660057_42660058insATCAGCCCTGGTTGG NCBI36
NG_027718.1:g.75018_75019insATCAGCCCTGGTTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+149_627+150insATCAGCCCTGGTTGG MANE Select ENSP00000382670.2:n.627+149_627+150insATCAGCCCTGGTTGG
ENST00000399770.2:c.627+149_627+150insATCAGCCCTGGTTGG ENSP00000382670.2:n.627+149_627+150insATCAGCCCTGGTTGG
NM_001080476.2:c.627+149_627+150insATCAGCCCTGGTTGG NP_001073945.1:n.627+149_627+150insATCAGCCCTGGTTGG
XM_011513691.1:c.264+149_264+150insATCAGCCCTGGTTGG XP_011511993.1:n.264+149_264+150insATCAGCCCTGGTTGG
NM_001080476.3:c.627+149_627+150insATCAGCCCTGGTTGG MANE Select NP_001073945.1:n.627+149_627+150insATCAGCCCTGGTTGG