Canonical Allele Identifier: CA2904512
Community Standard Title: NM_001080476.3(GRXCR1):c.700C>T (p.Gln234Ter)
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030367C>T , CM000666.2:g.43030367C>T GRCh38
NC_000004.11:g.43032384C>T , CM000666.1:g.43032384C>T GRCh37
NC_000004.10:g.42727141C>T NCBI36
NG_027718.1:g.142102C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001080476.3:c.700C>T MANE Select NP_001073945.1:p.Gln234Ter
ENST00000399770.3:c.700C>T MANE Select ENSP00000382670.2:p.Gln234Ter
NM_001080476.2:c.700C>T NP_001073945.1:p.Gln234Ter
ENST00000399770.2:c.700C>T ENSP00000382670.2:p.Gln234Ter
XM_011513691.1:c.337C>T XP_011511993.1:p.Gln113Ter