Canonical Allele Identifier: CA381462046

Gene: BBS1 ZDHHC24

Linked Data

• MyVariant Identifiers: chr11:g.66291209G>T (hg19) ; chr11:g.66523738G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66523738G>T , CM000673.2:g.66523738G>T	GRCh38
NC_000011.9:g.66291209G>T , CM000673.1:g.66291209G>T	GRCh37
NC_000011.8:g.66047785G>T	NCBI36
NG_009093.1:g.18091G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.966G>T (BBS1) MANE Select	ENSP00000317469.7:p.Trp322Cys
ENST00000318312.11:c.966G>T (BBS1)	ENSP00000317469.7:p.Trp322Cys
ENST00000393994.4:c.724-2385G>T (BBS1)	ENSP00000377563.2:n.724-2385G>T
ENST00000419755.3:c.1077G>T	ENSP00000398526.3:p.Trp359Cys
ENST00000455748.6:c.675G>T (BBS1)	ENSP00000405764.2:p.Trp225Cys
ENST00000526760.5:c.*673G>T (BBS1)	ENSP00000432140.1:n.*673G>T
ENST00000526986.5:c.*22-2272C>A (ZDHHC24)	ENSP00000431321.1:n.*22-2272C>A
ENST00000527959.1:n.110G>T (BBS1)
ENST00000529766.5:n.973G>T (BBS1)
ENST00000529895.1:n.415G>T (BBS1)
ENST00000529955.5:n.937G>T (BBS1)
ENST00000532908.5:c.*626G>T (BBS1)	ENSP00000431866.1:n.*626G>T
ENST00000534073.5:c.*143+417C>A (ZDHHC24)	ENSP00000436503.1:n.*143+417C>A
ENST00000630659.2:c.*673G>T (BBS1)	ENSP00000486455.1:n.*673G>T
NM_024649.4:c.966G>T (BBS1)	NP_078925.3:p.Trp322Cys
XM_005273874.3:c.*22-2272C>A (ZDHHC24)	XP_005273931.1:n.*22-2272C>A
XR_949860.1:n.808+417C>A (ZDHHC24)
NM_001348571.1:c.*22-2272C>A (ZDHHC24)	NP_001335500.1:n.*22-2272C>A
XM_005273874.4:c.*22-2272C>A (ZDHHC24)	XP_005273931.1:n.*22-2272C>A
XR_001747823.2:n.862+417C>A (ZDHHC24)
XR_949860.3:n.933+417C>A (ZDHHC24)
NM_024649.5:c.966G>T (BBS1) MANE Select	NP_078925.3:p.Trp322Cys
NM_001348571.2:c.*22-2272C>A (ZDHHC24)	NP_001335500.1:n.*22-2272C>A