Canonical Allele Identifier: CA2763339297

Gene: BBS7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121854909_121854912del , CM000666.2:g.121854909_121854912del	GRCh38
NC_000004.11:g.122776064_122776067del , CM000666.1:g.122776064_122776067del	GRCh37
NC_000004.10:g.122995514_122995517del	NCBI36
NG_009111.1:g.20576_20579del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264499.9:c.602-92_602-89del MANE Select	ENSP00000264499.4:n.602-92_602-89del
ENST00000264499.8:c.602-92_602-89del	ENSP00000264499.4:n.602-92_602-89del
ENST00000506636.1:c.602-92_602-89del	ENSP00000423626.1:n.602-92_602-89del
NM_018190.3:c.602-92_602-89del	NP_060660.2:n.602-92_602-89del
NM_176824.2:c.602-92_602-89del	NP_789794.1:n.602-92_602-89del
XM_005263106.2:c.602-89_602-86del	XP_005263163.1:n.602-89_602-86del
XM_011532079.1:c.647-89_647-86del	XP_011530381.1:n.647-89_647-86del
XM_011532080.1:c.647-92_647-89del	XP_011530382.1:n.647-92_647-89del
XM_011532081.1:c.647-89_647-86del	XP_011530383.1:n.647-89_647-86del
XM_005263106.4:c.602-89_602-86del	XP_005263163.1:n.602-89_602-86del
XM_011532079.3:c.647-89_647-86del	XP_011530381.1:n.647-89_647-86del
XM_011532080.3:c.647-92_647-89del	XP_011530382.1:n.647-92_647-89del
XM_011532081.3:c.647-89_647-86del	XP_011530383.1:n.647-89_647-86del
XM_017008357.2:c.602-92_602-89del	XP_016863846.1:n.602-92_602-89del
XM_017008358.2:c.602-89_602-86del	XP_016863847.1:n.602-89_602-86del
NM_176824.3:c.602-92_602-89del MANE Select	NP_789794.1:n.602-92_602-89del
NM_018190.4:c.602-92_602-89del	NP_060660.2:n.602-92_602-89del