Canonical Allele Identifier: CA645575838
Gene: SHBG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7630197_7630210del , CM000679.2:g.7630197_7630210del GRCh38
NC_000017.10:g.7533515_7533528del , CM000679.1:g.7533515_7533528del GRCh37
NC_000017.9:g.7474240_7474253del NCBI36
NG_011981.2:g.21134_21147del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380450.9:c.25_38del MANE Select ENSP00000369816.4:p.Thr9AlafsTer?
ENST00000340624.9:c.-63-219_-63-206del ENSP00000345675.6:n.-63-219_-63-206del
ENST00000380450.8:c.25_38del ENSP00000369816.4:p.Thr9AlafsTer?
ENST00000416273.7:c.25_38del ENSP00000388867.3:p.Thr9AlafsTer?
ENST00000441599.6:c.25_38del ENSP00000393426.2:p.Thr9AlafsTer?
ENST00000570353.5:c.25_38del ENSP00000458199.1:p.Thr9AlafsTer?
ENST00000570527.5:c.25_38del ENSP00000461162.1:p.Thr9AlafsTer?
ENST00000570547.5:c.-61-221_-61-208del ENSP00000458875.1:n.-61-221_-61-208del
ENST00000572182.5:c.-61-221_-61-208del ENSP00000458816.1:n.-61-221_-61-208del
ENST00000572262.5:c.-61-221_-61-208del ENSP00000459999.1:n.-61-221_-61-208del
ENST00000574539.5:c.-61-221_-61-208del ENSP00000458181.1:n.-61-221_-61-208del
ENST00000575314.5:c.-61-221_-61-208del ENSP00000458559.1:n.-61-221_-61-208del
ENST00000575729.5:c.-63-219_-63-206del ENSP00000458719.1:n.-63-219_-63-206del
ENST00000575903.5:c.25_38del ENSP00000458973.1:p.Thr9AlafsTer?
ENST00000576478.5:c.-61-221_-61-208del ENSP00000461133.1:n.-61-221_-61-208del
ENST00000576728.5:c.-61-221_-61-208del ENSP00000459620.1:n.-61-221_-61-208del
NM_001040.4:c.25_38del NP_001031.2:p.Thr9AlafsTer?
NM_001146279.2:c.25_38del NP_001139751.1:p.Thr9AlafsTer?
NM_001146280.2:c.25_38del NP_001139752.1:p.Thr9AlafsTer?
NM_001146281.2:c.25_38del NP_001139753.1:p.Thr9AlafsTer?
NM_001289113.1:c.-63-219_-63-206del NP_001276042.1:n.-63-219_-63-206del
NM_001289114.1:c.-61-221_-61-208del NP_001276043.1:n.-61-221_-61-208del
NM_001289115.1:c.-63-219_-63-206del NP_001276044.1:n.-63-219_-63-206del
NM_001289116.1:c.-232_-219del NP_001276045.1:n.-232_-219del
XM_011523991.1:c.25_38del XP_011522293.1:p.Thr9AlafsTer?
NM_001040.5:c.25_38del MANE Select NP_001031.2:p.Thr9AlafsTer?
NM_001146279.3:c.25_38del NP_001139751.1:p.Thr9AlafsTer?
NM_001146280.3:c.25_38del NP_001139752.1:p.Thr9AlafsTer?
NM_001289116.2:c.-232_-219del NP_001276045.1:n.-232_-219del
NM_001146281.3:c.25_38del NP_001139753.1:p.Thr9AlafsTer?
NM_001289113.2:c.-63-219_-63-206del NP_001276042.1:n.-63-219_-63-206del
NM_001289114.2:c.-61-221_-61-208del NP_001276043.1:n.-61-221_-61-208del
NM_001289115.2:c.-63-219_-63-206del NP_001276044.1:n.-63-219_-63-206del