Canonical Allele Identifier: CA2245918608
Gene: SHBG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7618443_7618461delinsGTTTTTTTTGTTTTTGTTT , CM000679.2:g.7618443_7618461delinsGTTTTTTTTGTTTTTGTTT GRCh38
NC_000017.10:g.7521761_7521779delinsGTTTTTTTTGTTTTTGTTT , CM000679.1:g.7521761_7521779delinsGTTTTTTTTGTTTTTGTTT GRCh37
NC_000017.9:g.7462486_7462504delinsGTTTTTTTTGTTTTTGTTT NCBI36
NG_011981.2:g.9380_9398delinsGTTTTTTTTGTTTTTGTTT
NG_028105.1:g.1437_1455delinsAAACAAAAACAAAAAAAAC , LRG_285:g.1437_1455delinsAAACAAAAACAAAAAAAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000570547.5:c.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTTT ENSP00000458875.1:n.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTT...
ENST00000572182.5:c.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTTT ENSP00000458816.1:n.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTT...
ENST00000572262.5:c.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTTT ENSP00000459999.1:n.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTT...
ENST00000574539.5:c.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTTT ENSP00000458181.1:n.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTT...
ENST00000575314.5:c.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTTT ENSP00000458559.1:n.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTT...
ENST00000576478.5:c.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTTT ENSP00000461133.1:n.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTT...
ENST00000576728.5:c.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTTT ENSP00000459620.1:n.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTT...
NM_001289114.1:c.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTTT NP_001276043.1:n.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTTT
NM_001289114.2:c.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTTT NP_001276043.1:n.-62+4332_-62+4350delinsGTTTTTTTTGTTTTTGTTT