Canonical Allele Identifier: CA381424038

Gene: BBS1 ZDHHC24

Linked Data

• COSMIC: COSM159342 ; COSM5784899
• MyVariant Identifiers: chr11:g.66297382C>G (hg19) ; chr11:g.66529911C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66529911C>G , CM000673.2:g.66529911C>G	GRCh38
NC_000011.9:g.66297382C>G , CM000673.1:g.66297382C>G	GRCh37
NC_000011.8:g.66053958C>G	NCBI36
NG_009093.1:g.24264C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.1432C>G (BBS1) MANE Select	ENSP00000317469.7:p.Leu478Val
ENST00000318312.11:c.1432C>G (BBS1)	ENSP00000317469.7:p.Leu478Val
ENST00000393994.4:c.1045C>G (BBS1)	ENSP00000377563.2:p.Leu349Val
ENST00000419755.3:c.1543C>G	ENSP00000398526.3:p.Leu515Val
ENST00000455748.6:c.1141C>G (BBS1)	ENSP00000405764.2:p.Leu381Val
ENST00000526760.5:c.*1139C>G (BBS1)	ENSP00000432140.1:n.*1139C>G
ENST00000526986.5:c.560-423G>C (ZDHHC24)	ENSP00000431321.1:n.560-423G>C
ENST00000529955.5:n.1403C>G (BBS1)
ENST00000534073.5:c.560-2905G>C (ZDHHC24)	ENSP00000436503.1:n.560-2905G>C
ENST00000630659.2:c.*1139C>G (BBS1)	ENSP00000486455.1:n.*1139C>G
NM_024649.4:c.1432C>G (BBS1)	NP_078925.3:p.Leu478Val
XM_005273874.3:c.560-2905G>C (ZDHHC24)	XP_005273931.1:n.560-2905G>C
XM_011544891.1:c.560-423G>C (ZDHHC24)	XP_011543193.1:n.560-423G>C
XM_011544894.1:c.560-2905G>C (ZDHHC24)	XP_011543196.1:n.560-2905G>C
XM_011544895.1:c.560-5635G>C (ZDHHC24)	XP_011543197.1:n.560-5635G>C
XR_949860.1:n.616-2905G>C (ZDHHC24)
NM_001348571.1:c.560-423G>C (ZDHHC24)	NP_001335500.1:n.560-423G>C
XM_005273874.4:c.560-2905G>C (ZDHHC24)	XP_005273931.1:n.560-2905G>C
XM_011544894.2:c.560-2905G>C (ZDHHC24)	XP_011543196.1:n.560-2905G>C
XR_001747823.2:n.741-5635G>C (ZDHHC24)
XR_949860.3:n.741-2905G>C (ZDHHC24)
NM_024649.5:c.1432C>G (BBS1) MANE Select	NP_078925.3:p.Leu478Val
NM_001348571.2:c.560-423G>C (ZDHHC24)	NP_001335500.1:n.560-423G>C