Canonical Allele Identifier: CA1453073968
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1748171788
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963354_42963356del , CM000666.2:g.42963354_42963356del GRCh38
NC_000004.11:g.42965371_42965373del , CM000666.1:g.42965371_42965373del GRCh37
NC_000004.10:g.42660128_42660130del NCBI36
NG_027718.1:g.75089_75091del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+220_627+222del MANE Select ENSP00000382670.2:n.627+220_627+222del
ENST00000399770.2:c.627+220_627+222del ENSP00000382670.2:n.627+220_627+222del
NM_001080476.2:c.627+220_627+222del NP_001073945.1:n.627+220_627+222del
XM_011513691.1:c.264+220_264+222del XP_011511993.1:n.264+220_264+222del
NM_001080476.3:c.627+220_627+222del MANE Select NP_001073945.1:n.627+220_627+222del
Search 100 bp 5'
Search 100 bp 3'