Canonical Allele Identifier: CA1490025974

Gene: BBS7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121854712T= , CM000666.2:g.121854712T=	GRCh38
NC_000004.11:g.122775867T= , CM000666.1:g.122775867T=	GRCh37
NC_000004.10:g.122995317T=	NCBI36
NG_009111.1:g.20776A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264499.9:c.710A= MANE Select	ENSP00000264499.4:p.Lys237=
ENST00000264499.8:c.710A=	ENSP00000264499.4:p.Lys237=
ENST00000506636.1:c.710A=	ENSP00000423626.1:p.Lys237=
NM_018190.3:c.710A=	NP_060660.2:p.Lys237=
NM_176824.2:c.710A=	NP_789794.1:p.Lys237=
XM_005263106.2:c.713A=	XP_005263163.1:p.Lys238=
XM_011532079.1:c.758A=	XP_011530381.1:p.Lys253=
XM_011532080.1:c.755A=	XP_011530382.1:p.Lys252=
XM_011532081.1:c.758A=	XP_011530383.1:p.Lys253=
XM_005263106.4:c.713A=	XP_005263163.1:p.Lys238=
XM_011532079.3:c.758A=	XP_011530381.1:p.Lys253=
XM_011532080.3:c.755A=	XP_011530382.1:p.Lys252=
XM_011532081.3:c.758A=	XP_011530383.1:p.Lys253=
XM_017008357.2:c.710A=	XP_016863846.1:p.Lys237=
XM_017008358.2:c.713A=	XP_016863847.1:p.Lys238=
NM_176824.3:c.710A= MANE Select	NP_789794.1:p.Lys237=
NM_018190.4:c.710A=	NP_060660.2:p.Lys237=