Canonical Allele Identifier: CA2521723338
Gene: GRXCR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962963_42962964insACT , CM000666.2:g.42962963_42962964insACT GRCh38
NC_000004.11:g.42964980_42964981insACT , CM000666.1:g.42964980_42964981insACT GRCh37
NC_000004.10:g.42659737_42659738insACT NCBI36
NG_027718.1:g.74698_74699insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.456_457insACT MANE Select ENSP00000382670.2:p.Thr152_Phe153insThr
ENST00000399770.2:c.456_457insACT ENSP00000382670.2:p.Thr152_Phe153insThr
NM_001080476.2:c.456_457insACT NP_001073945.1:p.Thr152_Phe153insThr
XM_011513691.1:c.93_94insACT XP_011511993.1:p.Thr31_Phe32insThr
NM_001080476.3:c.456_457insACT MANE Select NP_001073945.1:p.Thr152_Phe153insThr
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