Canonical Allele Identifier: CA2578076952
Gene: GRXCR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963175del , CM000666.2:g.42963175del GRCh38
NC_000004.11:g.42965192del , CM000666.1:g.42965192del GRCh37
NC_000004.10:g.42659949del NCBI36
NG_027718.1:g.74910del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+41del MANE Select ENSP00000382670.2:n.627+41del
ENST00000399770.2:c.627+41del ENSP00000382670.2:n.627+41del
NM_001080476.2:c.627+41del NP_001073945.1:n.627+41del
XM_011513691.1:c.264+41del XP_011511993.1:n.264+41del
NM_001080476.3:c.627+41del MANE Select NP_001073945.1:n.627+41del
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