Canonical Allele Identifier: CA381422083

Gene: BBS1 ZDHHC24

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66526121A>G , CM000673.2:g.66526121A>G	GRCh38
NC_000011.9:g.66293592A>G , CM000673.1:g.66293592A>G	GRCh37
NC_000011.8:g.66050168A>G	NCBI36
NG_009093.1:g.20474A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024649.5:c.1111-2A>G (BBS1) MANE Select	NP_078925.3:n.1111-2A>G
ENST00000318312.12:c.1111-2A>G (BBS1) MANE Select	ENSP00000317469.7:n.1111-2A>G
NM_001348571.1:c.*21+815T>C (ZDHHC24)	NP_001335500.1:n.*21+815T>C
NM_001348571.2:c.*21+815T>C (ZDHHC24)	NP_001335500.1:n.*21+815T>C
NM_024649.4:c.1111-2A>G (BBS1)	NP_078925.3:n.1111-2A>G
ENST00000318312.11:c.1111-2A>G (BBS1)	ENSP00000317469.7:n.1111-2A>G
ENST00000393994.4:c.724-2A>G (BBS1)	ENSP00000377563.2:n.724-2A>G
ENST00000419755.3:c.1222-2A>G	ENSP00000398526.3:n.1222-2A>G
ENST00000455748.6:c.820-2A>G (BBS1)	ENSP00000405764.2:n.820-2A>G
ENST00000526760.5:c.*818-2A>G (BBS1)	ENSP00000432140.1:n.*818-2A>G
ENST00000526986.5:c.*21+815T>C (ZDHHC24)	ENSP00000431321.1:n.*21+815T>C
ENST00000527959.1:n.255-2A>G (BBS1)
ENST00000529766.5:n.1118-2A>G (BBS1)
ENST00000529955.5:n.1082-2A>G (BBS1)
ENST00000534073.5:c.*21+815T>C (ZDHHC24)	ENSP00000436503.1:n.*21+815T>C
ENST00000630659.2:c.*818-2A>G (BBS1)	ENSP00000486455.1:n.*818-2A>G
XM_005273874.3:c.*21+815T>C (ZDHHC24)	XP_005273931.1:n.*21+815T>C
XM_005273874.4:c.*21+815T>C (ZDHHC24)	XP_005273931.1:n.*21+815T>C
XM_011544894.1:c.*22-561T>C (ZDHHC24)	XP_011543196.1:n.*22-561T>C
XM_011544894.2:c.*22-561T>C (ZDHHC24)	XP_011543196.1:n.*22-561T>C
XM_011544895.1:c.560-1845T>C (ZDHHC24)	XP_011543197.1:n.560-1845T>C
XR_001747823.2:n.741-1845T>C (ZDHHC24)
XR_949860.1:n.686+815T>C (ZDHHC24)
XR_949860.3:n.811+815T>C (ZDHHC24)