Canonical Allele Identifier: CA2576155058
Gene: SHBG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7630117_7630120dup , CM000679.2:g.7630117_7630120dup GRCh38
NC_000017.10:g.7533435_7533438dup , CM000679.1:g.7533435_7533438dup GRCh37
NC_000017.9:g.7474160_7474163dup NCBI36
NG_011981.2:g.21054_21057dup

Transcript Alleles

HGVS Amino-acid change
ENST00000340624.9:c.-63-299_-63-296dup ENSP00000345675.6:n.-63-299_-63-296dup
ENST00000441599.6:c.-56_-53dup ENSP00000393426.2:n.-56_-53dup
ENST00000570547.5:c.-61-301_-61-298dup ENSP00000458875.1:n.-61-301_-61-298dup
ENST00000572182.5:c.-61-301_-61-298dup ENSP00000458816.1:n.-61-301_-61-298dup
ENST00000572262.5:c.-61-301_-61-298dup ENSP00000459999.1:n.-61-301_-61-298dup
ENST00000574539.5:c.-61-301_-61-298dup ENSP00000458181.1:n.-61-301_-61-298dup
ENST00000575314.5:c.-61-301_-61-298dup ENSP00000458559.1:n.-61-301_-61-298dup
ENST00000575729.5:c.-63-299_-63-296dup ENSP00000458719.1:n.-63-299_-63-296dup
ENST00000576478.5:c.-61-301_-61-298dup ENSP00000461133.1:n.-61-301_-61-298dup
ENST00000576728.5:c.-61-301_-61-298dup ENSP00000459620.1:n.-61-301_-61-298dup
NM_001040.4:c.-56_-53dup NP_001031.2:n.-56_-53dup
NM_001146279.2:c.-56_-53dup NP_001139751.1:n.-56_-53dup
NM_001146280.2:c.-56_-53dup NP_001139752.1:n.-56_-53dup
NM_001146281.2:c.-56_-53dup NP_001139753.1:n.-56_-53dup
NM_001289113.1:c.-63-299_-63-296dup NP_001276042.1:n.-63-299_-63-296dup
NM_001289114.1:c.-61-301_-61-298dup NP_001276043.1:n.-61-301_-61-298dup
NM_001289115.1:c.-63-299_-63-296dup NP_001276044.1:n.-63-299_-63-296dup
NM_001289116.1:c.-312_-309dup NP_001276045.1:n.-312_-309dup
XM_011523991.1:c.-56_-53dup XP_011522293.1:n.-56_-53dup
NM_001289113.2:c.-63-299_-63-296dup NP_001276042.1:n.-63-299_-63-296dup
NM_001289114.2:c.-61-301_-61-298dup NP_001276043.1:n.-61-301_-61-298dup
NM_001289115.2:c.-63-299_-63-296dup NP_001276044.1:n.-63-299_-63-296dup