Canonical Allele Identifier: CA2245918684
Gene: SHBG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7618511_7618512delinsTG , CM000679.2:g.7618511_7618512delinsTG GRCh38
NC_000017.10:g.7521829_7521830delinsTG , CM000679.1:g.7521829_7521830delinsTG GRCh37
NC_000017.9:g.7462554_7462555delinsTG NCBI36
NG_011981.2:g.9448_9449delinsTG
NG_028105.1:g.1386_1387delinsCA , LRG_285:g.1386_1387delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000570547.5:c.-62+4400_-62+4401delinsTG ENSP00000458875.1:n.-62+4400_-62+4401delinsTG
ENST00000572182.5:c.-62+4400_-62+4401delinsTG ENSP00000458816.1:n.-62+4400_-62+4401delinsTG
ENST00000572262.5:c.-62+4400_-62+4401delinsTG ENSP00000459999.1:n.-62+4400_-62+4401delinsTG
ENST00000574539.5:c.-62+4400_-62+4401delinsTG ENSP00000458181.1:n.-62+4400_-62+4401delinsTG
ENST00000575314.5:c.-62+4400_-62+4401delinsTG ENSP00000458559.1:n.-62+4400_-62+4401delinsTG
ENST00000576478.5:c.-62+4400_-62+4401delinsTG ENSP00000461133.1:n.-62+4400_-62+4401delinsTG
ENST00000576728.5:c.-62+4400_-62+4401delinsTG ENSP00000459620.1:n.-62+4400_-62+4401delinsTG
NM_001289114.1:c.-62+4400_-62+4401delinsTG NP_001276043.1:n.-62+4400_-62+4401delinsTG
NM_001289114.2:c.-62+4400_-62+4401delinsTG NP_001276043.1:n.-62+4400_-62+4401delinsTG