Canonical Allele Identifier: CA1490026011

Gene: BBS7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121854808T= , CM000666.2:g.121854808T=	GRCh38
NC_000004.11:g.122775963T= , CM000666.1:g.122775963T=	GRCh37
NC_000004.10:g.122995413T=	NCBI36
NG_009111.1:g.20680A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264499.9:c.614A= MANE Select	ENSP00000264499.4:p.Glu205=
ENST00000264499.8:c.614A=	ENSP00000264499.4:p.Glu205=
ENST00000506636.1:c.614A=	ENSP00000423626.1:p.Glu205=
NM_018190.3:c.614A=	NP_060660.2:p.Glu205=
NM_176824.2:c.614A=	NP_789794.1:p.Glu205=
XM_005263106.2:c.617A=	XP_005263163.1:p.Glu206=
XM_011532079.1:c.662A=	XP_011530381.1:p.Glu221=
XM_011532080.1:c.659A=	XP_011530382.1:p.Glu220=
XM_011532081.1:c.662A=	XP_011530383.1:p.Glu221=
XM_005263106.4:c.617A=	XP_005263163.1:p.Glu206=
XM_011532079.3:c.662A=	XP_011530381.1:p.Glu221=
XM_011532080.3:c.659A=	XP_011530382.1:p.Glu220=
XM_011532081.3:c.662A=	XP_011530383.1:p.Glu221=
XM_017008357.2:c.614A=	XP_016863846.1:p.Glu205=
XM_017008358.2:c.617A=	XP_016863847.1:p.Glu206=
NM_176824.3:c.614A= MANE Select	NP_789794.1:p.Glu205=
NM_018190.4:c.614A=	NP_060660.2:p.Glu205=