Canonical Allele Identifier: CA2245927909
Gene: SHBG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7631270A= , CM000679.2:g.7631270A= GRCh38
NC_000017.10:g.7534588A= , CM000679.1:g.7534588A= GRCh37
NC_000017.9:g.7475313A= NCBI36
NG_011981.2:g.22207A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380450.9:c.464A= MANE Select ENSP00000369816.4:p.Gln155=
ENST00000340624.9:c.290A= ENSP00000345675.6:p.Gln97=
ENST00000380450.8:c.464A= ENSP00000369816.4:p.Gln155=
ENST00000416273.7:c.464A= ENSP00000388867.3:p.Gln155=
ENST00000441599.6:c.464A= ENSP00000393426.2:p.Gln155=
ENST00000570353.5:c.372A= ENSP00000458199.1:p.Thr124=
ENST00000570527.5:c.*422A= ENSP00000461162.1:n.*422A=
ENST00000570547.5:c.290A= ENSP00000458875.1:p.Gln97=
ENST00000571153.5:c.313-319A= ENSP00000458858.1:n.313-319A=
ENST00000572182.5:c.219+401A= ENSP00000458816.1:n.219+401A=
ENST00000572262.5:c.220-319A= ENSP00000459999.1:n.220-319A=
ENST00000574539.5:c.290A= ENSP00000458181.1:p.Gln97=
ENST00000575314.5:c.290A= ENSP00000458559.1:p.Gln97=
ENST00000575618.5:c.312+401A= ENSP00000459826.1:n.312+401A=
ENST00000575903.5:c.464A= ENSP00000458973.1:p.Gln155=
ENST00000576152.1:c.313-319A= ENSP00000461743.1:n.313-319A=
ENST00000576478.5:c.220-319A= ENSP00000461133.1:n.220-319A=
ENST00000576728.5:c.220-319A= ENSP00000459620.1:n.220-319A=
ENST00000576830.5:c.383A= ENSP00000460219.1:p.Gln128=
NM_001040.4:c.464A= NP_001031.2:p.Gln155=
NM_001146279.2:c.464A= NP_001139751.1:p.Gln155=
NM_001146280.2:c.464A= NP_001139752.1:p.Gln155=
NM_001146281.2:c.464A= NP_001139753.1:p.Gln155=
NM_001289113.1:c.290A= NP_001276042.1:p.Gln97=
NM_001289114.1:c.290A= NP_001276043.1:p.Gln97=
NM_001289115.1:c.290A= NP_001276044.1:p.Gln97=
NM_001289116.1:c.116A= NP_001276045.1:p.Gln39=
XM_011523991.1:c.464A= XP_011522293.1:p.Gln155=
NM_001040.5:c.464A= MANE Select NP_001031.2:p.Gln155=
NM_001146279.3:c.464A= NP_001139751.1:p.Gln155=
NM_001146280.3:c.464A= NP_001139752.1:p.Gln155=
NM_001289116.2:c.116A= NP_001276045.1:p.Gln39=
NM_001146281.3:c.464A= NP_001139753.1:p.Gln155=
NM_001289113.2:c.290A= NP_001276042.1:p.Gln97=
NM_001289114.2:c.290A= NP_001276043.1:p.Gln97=
NM_001289115.2:c.290A= NP_001276044.1:p.Gln97=