Canonical Allele Identifier: CA381462453

Gene: BBS1 ZDHHC24

Linked Data

• MyVariant Identifiers: chr11:g.66291289G>T (hg19) ; chr11:g.66523818G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66523818G>T , CM000673.2:g.66523818G>T	GRCh38
NC_000011.9:g.66291289G>T , CM000673.1:g.66291289G>T	GRCh37
NC_000011.8:g.66047865G>T	NCBI36
NG_009093.1:g.18171G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.1046G>T (BBS1) MANE Select	ENSP00000317469.7:p.Gly349Val
ENST00000318312.11:c.1046G>T (BBS1)	ENSP00000317469.7:p.Gly349Val
ENST00000393994.4:c.724-2305G>T (BBS1)	ENSP00000377563.2:n.724-2305G>T
ENST00000419755.3:c.1157G>T	ENSP00000398526.3:p.Gly386Val
ENST00000455748.6:c.755G>T (BBS1)	ENSP00000405764.2:p.Gly252Val
ENST00000526760.5:c.*753G>T (BBS1)	ENSP00000432140.1:n.*753G>T
ENST00000526986.5:c.*22-2352C>A (ZDHHC24)	ENSP00000431321.1:n.*22-2352C>A
ENST00000527959.1:n.190G>T (BBS1)
ENST00000529766.5:n.1053G>T (BBS1)
ENST00000529895.1:n.495G>T (BBS1)
ENST00000529955.5:n.1017G>T (BBS1)
ENST00000532908.5:c.*706G>T (BBS1)	ENSP00000431866.1:n.*706G>T
ENST00000534073.5:c.*143+337C>A (ZDHHC24)	ENSP00000436503.1:n.*143+337C>A
ENST00000630659.2:c.*753G>T (BBS1)	ENSP00000486455.1:n.*753G>T
NM_024649.4:c.1046G>T (BBS1)	NP_078925.3:p.Gly349Val
XM_005273874.3:c.*22-2352C>A (ZDHHC24)	XP_005273931.1:n.*22-2352C>A
XR_949860.1:n.808+337C>A (ZDHHC24)
NM_001348571.1:c.*22-2352C>A (ZDHHC24)	NP_001335500.1:n.*22-2352C>A
XM_005273874.4:c.*22-2352C>A (ZDHHC24)	XP_005273931.1:n.*22-2352C>A
XR_001747823.2:n.862+337C>A (ZDHHC24)
XR_949860.3:n.933+337C>A (ZDHHC24)
NM_024649.5:c.1046G>T (BBS1) MANE Select	NP_078925.3:p.Gly349Val
NM_001348571.2:c.*22-2352C>A (ZDHHC24)	NP_001335500.1:n.*22-2352C>A