Canonical Allele Identifier: CA1490025899

Gene: BBS7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121854540_121854543delinsCAAT , CM000666.2:g.121854540_121854543delinsCAAT	GRCh38
NC_000004.11:g.122775695_122775698delinsCAAT , CM000666.1:g.122775695_122775698delinsCAAT	GRCh37
NC_000004.10:g.122995145_122995148delinsCAAT	NCBI36
NG_009111.1:g.20945_20948delinsATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264499.9:c.718+161_718+164delinsATTG MANE Select	ENSP00000264499.4:n.718+161_718+164delinsATTG
ENST00000264499.8:c.718+161_718+164delinsATTG	ENSP00000264499.4:n.718+161_718+164delinsATTG
ENST00000506636.1:c.718+161_718+164delinsATTG	ENSP00000423626.1:n.718+161_718+164delinsATTG
NM_018190.3:c.718+161_718+164delinsATTG	NP_060660.2:n.718+161_718+164delinsATTG
NM_176824.2:c.718+161_718+164delinsATTG	NP_789794.1:n.718+161_718+164delinsATTG
XM_005263106.2:c.721+161_721+164delinsATTG	XP_005263163.1:n.721+161_721+164delinsATTG
XM_011532079.1:c.766+161_766+164delinsATTG	XP_011530381.1:n.766+161_766+164delinsATTG
XM_011532080.1:c.763+161_763+164delinsATTG	XP_011530382.1:n.763+161_763+164delinsATTG
XM_011532081.1:c.766+161_766+164delinsATTG	XP_011530383.1:n.766+161_766+164delinsATTG
XM_005263106.4:c.721+161_721+164delinsATTG	XP_005263163.1:n.721+161_721+164delinsATTG
XM_011532079.3:c.766+161_766+164delinsATTG	XP_011530381.1:n.766+161_766+164delinsATTG
XM_011532080.3:c.763+161_763+164delinsATTG	XP_011530382.1:n.763+161_763+164delinsATTG
XM_011532081.3:c.766+161_766+164delinsATTG	XP_011530383.1:n.766+161_766+164delinsATTG
XM_017008357.2:c.718+161_718+164delinsATTG	XP_016863846.1:n.718+161_718+164delinsATTG
XM_017008358.2:c.721+161_721+164delinsATTG	XP_016863847.1:n.721+161_721+164delinsATTG
NM_176824.3:c.718+161_718+164delinsATTG MANE Select	NP_789794.1:n.718+161_718+164delinsATTG
NM_018190.4:c.718+161_718+164delinsATTG	NP_060660.2:n.718+161_718+164delinsATTG