Canonical Allele Identifier: CA6123748

Gene: BBS1 ZDHHC24

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66529850C>T , CM000673.2:g.66529850C>T	GRCh38
NC_000011.9:g.66297321C>T , CM000673.1:g.66297321C>T	GRCh37
NC_000011.8:g.66053897C>T	NCBI36
NG_009093.1:g.24203C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024649.5:c.1371C>T (BBS1) MANE Select	NP_078925.3:p.Tyr457=
ENST00000318312.12:c.1371C>T (BBS1) MANE Select	ENSP00000317469.7:p.Tyr457=
NM_001348571.1:c.560-362G>A (ZDHHC24)	NP_001335500.1:n.560-362G>A
NM_001348571.2:c.560-362G>A (ZDHHC24)	NP_001335500.1:n.560-362G>A
NM_024649.4:c.1371C>T (BBS1)	NP_078925.3:p.Tyr457=
ENST00000318312.11:c.1371C>T (BBS1)	ENSP00000317469.7:p.Tyr457=
ENST00000393994.4:c.984C>T (BBS1)	ENSP00000377563.2:p.Tyr328=
ENST00000419755.3:c.1482C>T	ENSP00000398526.3:p.Tyr494=
ENST00000455748.6:c.1080C>T (BBS1)	ENSP00000405764.2:p.Tyr360=
ENST00000526760.5:c.*1078C>T (BBS1)	ENSP00000432140.1:n.*1078C>T
ENST00000526986.5:c.560-362G>A (ZDHHC24)	ENSP00000431321.1:n.560-362G>A
ENST00000529955.5:n.1342C>T (BBS1)
ENST00000534073.5:c.560-2844G>A (ZDHHC24)	ENSP00000436503.1:n.560-2844G>A
ENST00000630659.2:c.*1078C>T (BBS1)	ENSP00000486455.1:n.*1078C>T
XM_005273874.3:c.560-2844G>A (ZDHHC24)	XP_005273931.1:n.560-2844G>A
XM_005273874.4:c.560-2844G>A (ZDHHC24)	XP_005273931.1:n.560-2844G>A
XM_011544891.1:c.560-362G>A (ZDHHC24)	XP_011543193.1:n.560-362G>A
XM_011544894.1:c.560-2844G>A (ZDHHC24)	XP_011543196.1:n.560-2844G>A
XM_011544894.2:c.560-2844G>A (ZDHHC24)	XP_011543196.1:n.560-2844G>A
XM_011544895.1:c.560-5574G>A (ZDHHC24)	XP_011543197.1:n.560-5574G>A
XR_001747823.2:n.741-5574G>A (ZDHHC24)
XR_949860.1:n.616-2844G>A (ZDHHC24)
XR_949860.3:n.741-2844G>A (ZDHHC24)