Canonical Allele Identifier: CA2245888590
Community Standard Title: NM_001040.5(SHBG):c.1066G= (p.Asp356=)
Gene: SHBG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7633209G= , CM000679.2:g.7633209G= GRCh38
NC_000017.10:g.7536527G= , CM000679.1:g.7536527G= GRCh37
NC_000017.9:g.7477252G= NCBI36
NG_011981.2:g.24146G=

Transcript Alleles

HGVS Amino-acid Change
NM_001040.5:c.1066G= MANE Select NP_001031.2:p.Asp356=
ENST00000380450.9:c.1066G= MANE Select ENSP00000369816.4:p.Asp356=
NM_001040.4:c.1066G= NP_001031.2:p.Asp356=
NM_001146279.2:c.1012G= NP_001139751.1:p.Asp338=
NM_001146279.3:c.1012G= NP_001139751.1:p.Asp338=
NM_001146280.2:c.858G= NP_001139752.1:p.Lys286=
NM_001146280.3:c.858G= NP_001139752.1:p.Lys286=
NM_001146281.2:c.721G= NP_001139753.1:p.Asp241=
NM_001146281.3:c.721G= NP_001139753.1:p.Asp241=
NM_001289113.1:c.892G= NP_001276042.1:p.Asp298=
NM_001289113.2:c.892G= NP_001276042.1:p.Asp298=
NM_001289114.1:c.892G= NP_001276043.1:p.Asp298=
NM_001289114.2:c.892G= NP_001276043.1:p.Asp298=
NM_001289115.1:c.684G= NP_001276044.1:p.Lys228=
NM_001289115.2:c.684G= NP_001276044.1:p.Lys228=
NM_001289116.1:c.718G= NP_001276045.1:p.Asp240=
NM_001289116.2:c.718G= NP_001276045.1:p.Asp240=
ENST00000340624.9:c.892G= ENSP00000345675.6:p.Asp298=
ENST00000380450.8:c.1066G= ENSP00000369816.4:p.Asp356=
ENST00000416273.7:c.858G= ENSP00000388867.3:p.Lys286=
ENST00000441599.6:c.721G= ENSP00000393426.2:p.Asp241=
ENST00000570353.5:c.*428G= ENSP00000458199.1:n.*428G=
ENST00000570527.5:c.*1024G= ENSP00000461162.1:n.*1024G=
ENST00000570547.5:c.547G= ENSP00000458875.1:p.Asp183=
ENST00000571153.5:c.615G= ENSP00000458858.1:p.Lys205=
ENST00000572182.5:c.225G= ENSP00000458816.1:p.Lys75=
ENST00000572262.5:c.730G= ENSP00000459999.1:p.Asp244=
ENST00000574539.5:c.684G= ENSP00000458181.1:p.Lys228=
ENST00000575314.5:c.892G= ENSP00000458559.1:p.Asp298=
ENST00000575618.5:c.318G= ENSP00000459826.1:p.Lys106=
ENST00000575903.5:c.1012G= ENSP00000458973.1:p.Asp338=
ENST00000576152.1:c.478G= ENSP00000461743.1:p.Asp160=
ENST00000576478.5:c.385G= ENSP00000461133.1:p.Asp129=
ENST00000576728.5:c.522G= ENSP00000459620.1:p.Lys174=
ENST00000576830.5:c.640G= ENSP00000460219.1:p.Asp214=