Canonical Allele Identifier: CA2670496568
Gene: GRXCR1 HGNC NCBI

Linked Data

gnomAD v4: 4-42963270-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963271del , CM000666.2:g.42963271del GRCh38
NC_000004.11:g.42965288del , CM000666.1:g.42965288del GRCh37
NC_000004.10:g.42660045del NCBI36
NG_027718.1:g.75006del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+137del MANE Select ENSP00000382670.2:n.627+137del
ENST00000399770.2:c.627+137del ENSP00000382670.2:n.627+137del
NM_001080476.2:c.627+137del NP_001073945.1:n.627+137del
XM_011513691.1:c.264+137del XP_011511993.1:n.264+137del
NM_001080476.3:c.627+137del MANE Select NP_001073945.1:n.627+137del
Search 100 bp 5'
Search 100 bp 3'