Canonical Allele Identifier: CA1490015308

Gene: BBS7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121828177T= , CM000666.2:g.121828177T=	GRCh38
NC_000004.11:g.122749332T= , CM000666.1:g.122749332T=	GRCh37
NC_000004.10:g.122968782T=	NCBI36
NG_009111.1:g.47311A=
NG_052974.1:g.825A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264499.9:c.1983A= MANE Select	ENSP00000264499.4:p.Lys661=
ENST00000264499.8:c.1983A=	ENSP00000264499.4:p.Lys661=
ENST00000506636.1:c.1983A=	ENSP00000423626.1:p.Lys661=
ENST00000507814.5:c.252A=	ENSP00000423250.1:p.Lys84=
NM_018190.3:c.1983A=	NP_060660.2:p.Lys661=
NM_176824.2:c.1983A=	NP_789794.1:p.Lys661=
XM_005263106.2:c.1986A=	XP_005263163.1:p.Lys662=
XM_011532079.1:c.2031A=	XP_011530381.1:p.Lys677=
XM_011532080.1:c.2028A=	XP_011530382.1:p.Lys676=
XM_011532081.1:c.1866A=	XP_011530383.1:p.Lys622=
XM_005263106.4:c.1986A=	XP_005263163.1:p.Lys662=
XM_011532079.3:c.2031A=	XP_011530381.1:p.Lys677=
XM_011532080.3:c.2028A=	XP_011530382.1:p.Lys676=
XM_011532081.3:c.1866A=	XP_011530383.1:p.Lys622=
XM_017008357.2:c.1818A=	XP_016863846.1:p.Lys606=
XM_017008358.2:c.1821A=	XP_016863847.1:p.Lys607=
NM_176824.3:c.1983A= MANE Select	NP_789794.1:p.Lys661=
NM_018190.4:c.1983A=	NP_060660.2:p.Lys661=