Canonical Allele Identifier: CA2980005650
Community Standard Title: NM_001080476.3(GRXCR1):c.694-5T>G
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030356T>G , CM000666.2:g.43030356T>G GRCh38
NC_000004.11:g.43032373T>G , CM000666.1:g.43032373T>G GRCh37
NC_000004.10:g.42727130T>G NCBI36
NG_027718.1:g.142091T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001080476.3:c.694-5T>G MANE Select NP_001073945.1:n.694-5T>G
ENST00000399770.3:c.694-5T>G MANE Select ENSP00000382670.2:n.694-5T>G
NM_001080476.2:c.694-5T>G NP_001073945.1:n.694-5T>G
ENST00000399770.2:c.694-5T>G ENSP00000382670.2:n.694-5T>G
XM_011513691.1:c.331-5T>G XP_011511993.1:n.331-5T>G