Canonical Allele Identifier: CA2761203895
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963183_42963184insATGTTTTTCTCTTCAAATTTTACGC , CM000666.2:g.42963183_42963184insATGTTTTTCTCTTCAAATTTTACGC GRCh38
NC_000004.11:g.42965200_42965201insATGTTTTTCTCTTCAAATTTTACGC , CM000666.1:g.42965200_42965201insATGTTTTTCTCTTCAAATTTTACGC GRCh37
NC_000004.10:g.42659957_42659958insATGTTTTTCTCTTCAAATTTTACGC NCBI36
NG_027718.1:g.74918_74919insATGTTTTTCTCTTCAAATTTTACGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+49_627+50insATGTTTTTCTCTTCAAATTTTACGC MANE Select ENSP00000382670.2:n.627+49_627+50insATGTTTTTCTCTTCAAATTTTACGC...
ENST00000399770.2:c.627+49_627+50insATGTTTTTCTCTTCAAATTTTACGC ENSP00000382670.2:n.627+49_627+50insATGTTTTTCTCTTCAAATTTTACGC...
NM_001080476.2:c.627+49_627+50insATGTTTTTCTCTTCAAATTTTACGC NP_001073945.1:n.627+49_627+50insATGTTTTTCTCTTCAAATTTTACGC
XM_011513691.1:c.264+49_264+50insATGTTTTTCTCTTCAAATTTTACGC XP_011511993.1:n.264+49_264+50insATGTTTTTCTCTTCAAATTTTACGC
NM_001080476.3:c.627+49_627+50insATGTTTTTCTCTTCAAATTTTACGC MANE Select NP_001073945.1:n.627+49_627+50insATGTTTTTCTCTTCAAATTTTACGC