Canonical Allele Identifier: CA2245918628
Gene: SHBG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7618451_7618452delinsTG , CM000679.2:g.7618451_7618452delinsTG GRCh38
NC_000017.10:g.7521769_7521770delinsTG , CM000679.1:g.7521769_7521770delinsTG GRCh37
NC_000017.9:g.7462494_7462495delinsTG NCBI36
NG_011981.2:g.9388_9389delinsTG
NG_028105.1:g.1446_1447delinsCA , LRG_285:g.1446_1447delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000570547.5:c.-62+4340_-62+4341delinsTG ENSP00000458875.1:n.-62+4340_-62+4341delinsTG
ENST00000572182.5:c.-62+4340_-62+4341delinsTG ENSP00000458816.1:n.-62+4340_-62+4341delinsTG
ENST00000572262.5:c.-62+4340_-62+4341delinsTG ENSP00000459999.1:n.-62+4340_-62+4341delinsTG
ENST00000574539.5:c.-62+4340_-62+4341delinsTG ENSP00000458181.1:n.-62+4340_-62+4341delinsTG
ENST00000575314.5:c.-62+4340_-62+4341delinsTG ENSP00000458559.1:n.-62+4340_-62+4341delinsTG
ENST00000576478.5:c.-62+4340_-62+4341delinsTG ENSP00000461133.1:n.-62+4340_-62+4341delinsTG
ENST00000576728.5:c.-62+4340_-62+4341delinsTG ENSP00000459620.1:n.-62+4340_-62+4341delinsTG
NM_001289114.1:c.-62+4340_-62+4341delinsTG NP_001276043.1:n.-62+4340_-62+4341delinsTG
NM_001289114.2:c.-62+4340_-62+4341delinsTG NP_001276043.1:n.-62+4340_-62+4341delinsTG