Canonical Allele Identifier: CA2670496573
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963277_42963283del , CM000666.2:g.42963277_42963283del GRCh38
NC_000004.11:g.42965294_42965300del , CM000666.1:g.42965294_42965300del GRCh37
NC_000004.10:g.42660051_42660057del NCBI36
NG_027718.1:g.75012_75018del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+143_627+149del MANE Select ENSP00000382670.2:n.627+143_627+149del
ENST00000399770.2:c.627+143_627+149del ENSP00000382670.2:n.627+143_627+149del
NM_001080476.2:c.627+143_627+149del NP_001073945.1:n.627+143_627+149del
XM_011513691.1:c.264+143_264+149del XP_011511993.1:n.264+143_264+149del
NM_001080476.3:c.627+143_627+149del MANE Select NP_001073945.1:n.627+143_627+149del