Canonical Allele Identifier: CA1453073691
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962815_42962816delinsAT , CM000666.2:g.42962815_42962816delinsAT GRCh38
NC_000004.11:g.42964832_42964833delinsAT , CM000666.1:g.42964832_42964833delinsAT GRCh37
NC_000004.10:g.42659589_42659590delinsAT NCBI36
NG_027718.1:g.74550_74551delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.385-77_385-76delinsAT MANE Select ENSP00000382670.2:n.385-77_385-76delinsAT
ENST00000399770.2:c.385-77_385-76delinsAT ENSP00000382670.2:n.385-77_385-76delinsAT
NM_001080476.2:c.385-77_385-76delinsAT NP_001073945.1:n.385-77_385-76delinsAT
XM_011513691.1:c.22-77_22-76delinsAT XP_011511993.1:n.22-77_22-76delinsAT
NM_001080476.3:c.385-77_385-76delinsAT MANE Select NP_001073945.1:n.385-77_385-76delinsAT