Canonical Allele Identifier: CA2245927364

Gene: SHBG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7630145T= , CM000679.2:g.7630145T=	GRCh38
NC_000017.10:g.7533463T= , CM000679.1:g.7533463T=	GRCh37
NC_000017.9:g.7474188T=	NCBI36
NG_011981.2:g.21082T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380450.9:c.-28T= MANE Select	ENSP00000369816.4:n.-28T=
ENST00000340624.9:c.-63-271T=	ENSP00000345675.6:n.-63-271T=
ENST00000380450.8:c.-28T=	ENSP00000369816.4:n.-28T=
ENST00000441599.6:c.-28T=	ENSP00000393426.2:n.-28T=
ENST00000570547.5:c.-61-273T=	ENSP00000458875.1:n.-61-273T=
ENST00000572182.5:c.-61-273T=	ENSP00000458816.1:n.-61-273T=
ENST00000572262.5:c.-61-273T=	ENSP00000459999.1:n.-61-273T=
ENST00000574539.5:c.-61-273T=	ENSP00000458181.1:n.-61-273T=
ENST00000575314.5:c.-61-273T=	ENSP00000458559.1:n.-61-273T=
ENST00000575729.5:c.-63-271T=	ENSP00000458719.1:n.-63-271T=
ENST00000576478.5:c.-61-273T=	ENSP00000461133.1:n.-61-273T=
ENST00000576728.5:c.-61-273T=	ENSP00000459620.1:n.-61-273T=
NM_001040.4:c.-28T=	NP_001031.2:n.-28T=
NM_001146279.2:c.-28T=	NP_001139751.1:n.-28T=
NM_001146280.2:c.-28T=	NP_001139752.1:n.-28T=
NM_001146281.2:c.-28T=	NP_001139753.1:n.-28T=
NM_001289113.1:c.-63-271T=	NP_001276042.1:n.-63-271T=
NM_001289114.1:c.-61-273T=	NP_001276043.1:n.-61-273T=
NM_001289115.1:c.-63-271T=	NP_001276044.1:n.-63-271T=
NM_001289116.1:c.-284T=	NP_001276045.1:n.-284T=
XM_011523991.1:c.-28T=	XP_011522293.1:n.-28T=
NM_001040.5:c.-28T= MANE Select	NP_001031.2:n.-28T=
NM_001146279.3:c.-28T=	NP_001139751.1:n.-28T=
NM_001146280.3:c.-28T=	NP_001139752.1:n.-28T=
NM_001289116.2:c.-284T=	NP_001276045.1:n.-284T=
NM_001146281.3:c.-28T=	NP_001139753.1:n.-28T=
NM_001289113.2:c.-63-271T=	NP_001276042.1:n.-63-271T=
NM_001289114.2:c.-61-273T=	NP_001276043.1:n.-61-273T=
NM_001289115.2:c.-63-271T=	NP_001276044.1:n.-63-271T=