Canonical Allele Identifier: CA1453073961
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963345_42963346delinsCA , CM000666.2:g.42963345_42963346delinsCA GRCh38
NC_000004.11:g.42965362_42965363delinsCA , CM000666.1:g.42965362_42965363delinsCA GRCh37
NC_000004.10:g.42660119_42660120delinsCA NCBI36
NG_027718.1:g.75080_75081delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+211_627+212delinsCA MANE Select ENSP00000382670.2:n.627+211_627+212delinsCA
ENST00000399770.2:c.627+211_627+212delinsCA ENSP00000382670.2:n.627+211_627+212delinsCA
NM_001080476.2:c.627+211_627+212delinsCA NP_001073945.1:n.627+211_627+212delinsCA
XM_011513691.1:c.264+211_264+212delinsCA XP_011511993.1:n.264+211_264+212delinsCA
NM_001080476.3:c.627+211_627+212delinsCA MANE Select NP_001073945.1:n.627+211_627+212delinsCA