Canonical Allele Identifier: CA381422849

Gene: BBS1 ZDHHC24

Linked Data

• MyVariant Identifiers: chr11:g.66294239T>C (hg19) ; chr11:g.66526768T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66526768T>C , CM000673.2:g.66526768T>C	GRCh38
NC_000011.9:g.66294239T>C , CM000673.1:g.66294239T>C	GRCh37
NC_000011.8:g.66050815T>C	NCBI36
NG_009093.1:g.21121T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.1300T>C (BBS1) MANE Select	ENSP00000317469.7:p.Tyr434His
ENST00000318312.11:c.1300T>C (BBS1)	ENSP00000317469.7:p.Tyr434His
ENST00000393994.4:c.913T>C (BBS1)	ENSP00000377563.2:p.Tyr305His
ENST00000419755.3:c.1411T>C	ENSP00000398526.3:p.Tyr471His
ENST00000455748.6:c.1009T>C (BBS1)	ENSP00000405764.2:p.Tyr337His
ENST00000526760.5:c.*1007T>C (BBS1)	ENSP00000432140.1:n.*1007T>C
ENST00000526986.5:c.*21+168A>G (ZDHHC24)	ENSP00000431321.1:n.*21+168A>G
ENST00000527959.1:n.444T>C (BBS1)
ENST00000529766.5:n.1307T>C (BBS1)
ENST00000529955.5:n.1271T>C (BBS1)
ENST00000534073.5:c.*21+168A>G (ZDHHC24)	ENSP00000436503.1:n.*21+168A>G
ENST00000630659.2:c.*1007T>C (BBS1)	ENSP00000486455.1:n.*1007T>C
NM_024649.4:c.1300T>C (BBS1)	NP_078925.3:p.Tyr434His
XM_005273874.3:c.*21+168A>G (ZDHHC24)	XP_005273931.1:n.*21+168A>G
XM_011544894.1:c.*21+168A>G (ZDHHC24)	XP_011543196.1:n.*21+168A>G
XM_011544895.1:c.560-2492A>G (ZDHHC24)	XP_011543197.1:n.560-2492A>G
XR_949860.1:n.686+168A>G (ZDHHC24)
NM_001348571.1:c.*21+168A>G (ZDHHC24)	NP_001335500.1:n.*21+168A>G
XM_005273874.4:c.*21+168A>G (ZDHHC24)	XP_005273931.1:n.*21+168A>G
XM_011544894.2:c.*21+168A>G (ZDHHC24)	XP_011543196.1:n.*21+168A>G
XR_001747823.2:n.741-2492A>G (ZDHHC24)
XR_949860.3:n.811+168A>G (ZDHHC24)
NM_024649.5:c.1300T>C (BBS1) MANE Select	NP_078925.3:p.Tyr434His
NM_001348571.2:c.*21+168A>G (ZDHHC24)	NP_001335500.1:n.*21+168A>G