Canonical Allele Identifier: CA2670496527
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963219dup , CM000666.2:g.42963219dup GRCh38
NC_000004.11:g.42965236dup , CM000666.1:g.42965236dup GRCh37
NC_000004.10:g.42659993dup NCBI36
NG_027718.1:g.74954dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+85dup MANE Select ENSP00000382670.2:n.627+85dup
ENST00000399770.2:c.627+85dup ENSP00000382670.2:n.627+85dup
NM_001080476.2:c.627+85dup NP_001073945.1:n.627+85dup
XM_011513691.1:c.264+85dup XP_011511993.1:n.264+85dup
NM_001080476.3:c.627+85dup MANE Select NP_001073945.1:n.627+85dup