Canonical Allele Identifier: CA2671949238
Gene: BBS7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121854923_121854929del , CM000666.2:g.121854923_121854929del GRCh38
NC_000004.11:g.122776078_122776084del , CM000666.1:g.122776078_122776084del GRCh37
NC_000004.10:g.122995528_122995534del NCBI36
NG_009111.1:g.20559_20565del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264499.9:c.602-109_602-103del MANE Select ENSP00000264499.4:n.602-109_602-103del
ENST00000264499.8:c.602-109_602-103del ENSP00000264499.4:n.602-109_602-103del
ENST00000506636.1:c.602-109_602-103del ENSP00000423626.1:n.602-109_602-103del
NM_018190.3:c.602-109_602-103del NP_060660.2:n.602-109_602-103del
NM_176824.2:c.602-109_602-103del NP_789794.1:n.602-109_602-103del
XM_005263106.2:c.602-106_602-100del XP_005263163.1:n.602-106_602-100del
XM_011532079.1:c.647-106_647-100del XP_011530381.1:n.647-106_647-100del
XM_011532080.1:c.647-109_647-103del XP_011530382.1:n.647-109_647-103del
XM_011532081.1:c.647-106_647-100del XP_011530383.1:n.647-106_647-100del
XM_005263106.4:c.602-106_602-100del XP_005263163.1:n.602-106_602-100del
XM_011532079.3:c.647-106_647-100del XP_011530381.1:n.647-106_647-100del
XM_011532080.3:c.647-109_647-103del XP_011530382.1:n.647-109_647-103del
XM_011532081.3:c.647-106_647-100del XP_011530383.1:n.647-106_647-100del
XM_017008357.2:c.602-109_602-103del XP_016863846.1:n.602-109_602-103del
XM_017008358.2:c.602-106_602-100del XP_016863847.1:n.602-106_602-100del
NM_176824.3:c.602-109_602-103del MANE Select NP_789794.1:n.602-109_602-103del
NM_018190.4:c.602-109_602-103del NP_060660.2:n.602-109_602-103del