Canonical Allele Identifier: CA1490026097

Gene: BBS7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121855032G= , CM000666.2:g.121855032G=	GRCh38
NC_000004.11:g.122776187G= , CM000666.1:g.122776187G=	GRCh37
NC_000004.10:g.122995637G=	NCBI36
NG_009111.1:g.20456C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264499.9:c.602-212C= MANE Select	ENSP00000264499.4:n.602-212C=
ENST00000264499.8:c.602-212C=	ENSP00000264499.4:n.602-212C=
ENST00000506636.1:c.602-212C=	ENSP00000423626.1:n.602-212C=
NM_018190.3:c.602-212C=	NP_060660.2:n.602-212C=
NM_176824.2:c.602-212C=	NP_789794.1:n.602-212C=
XM_005263106.2:c.602-209C=	XP_005263163.1:n.602-209C=
XM_011532079.1:c.647-209C=	XP_011530381.1:n.647-209C=
XM_011532080.1:c.647-212C=	XP_011530382.1:n.647-212C=
XM_011532081.1:c.647-209C=	XP_011530383.1:n.647-209C=
XM_005263106.4:c.602-209C=	XP_005263163.1:n.602-209C=
XM_011532079.3:c.647-209C=	XP_011530381.1:n.647-209C=
XM_011532080.3:c.647-212C=	XP_011530382.1:n.647-212C=
XM_011532081.3:c.647-209C=	XP_011530383.1:n.647-209C=
XM_017008357.2:c.602-212C=	XP_016863846.1:n.602-212C=
XM_017008358.2:c.602-209C=	XP_016863847.1:n.602-209C=
NM_176824.3:c.602-212C= MANE Select	NP_789794.1:n.602-212C=
NM_018190.4:c.602-212C=	NP_060660.2:n.602-212C=