Canonical Allele Identifier: CA2670496543
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963239_42963240insT , CM000666.2:g.42963239_42963240insT GRCh38
NC_000004.11:g.42965256_42965257insT , CM000666.1:g.42965256_42965257insT GRCh37
NC_000004.10:g.42660013_42660014insT NCBI36
NG_027718.1:g.74974_74975insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+105_627+106insT MANE Select ENSP00000382670.2:n.627+105_627+106insT
ENST00000399770.2:c.627+105_627+106insT ENSP00000382670.2:n.627+105_627+106insT
NM_001080476.2:c.627+105_627+106insT NP_001073945.1:n.627+105_627+106insT
XM_011513691.1:c.264+105_264+106insT XP_011511993.1:n.264+105_264+106insT
NM_001080476.3:c.627+105_627+106insT MANE Select NP_001073945.1:n.627+105_627+106insT