Canonical Allele Identifier: CA2670496560
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963264_42963265dup , CM000666.2:g.42963264_42963265dup GRCh38
NC_000004.11:g.42965281_42965282dup , CM000666.1:g.42965281_42965282dup GRCh37
NC_000004.10:g.42660038_42660039dup NCBI36
NG_027718.1:g.74999_75000dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+130_627+131dup MANE Select ENSP00000382670.2:n.627+130_627+131dup
ENST00000399770.2:c.627+130_627+131dup ENSP00000382670.2:n.627+130_627+131dup
NM_001080476.2:c.627+130_627+131dup NP_001073945.1:n.627+130_627+131dup
XM_011513691.1:c.264+130_264+131dup XP_011511993.1:n.264+130_264+131dup
NM_001080476.3:c.627+130_627+131dup MANE Select NP_001073945.1:n.627+130_627+131dup