Canonical Allele Identifier: CA381462034

Gene: BBS1 ZDHHC24

Linked Data

• ClinVar Variation Id: 983997
• ClinVar RCV Id: RCV001264002
• dbSNP Id: rs1856354695
• MyVariant Identifiers: chr11:g.66291208G>A (hg19) ; chr11:g.66523737G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66523737G>A , CM000673.2:g.66523737G>A	GRCh38
NC_000011.9:g.66291208G>A , CM000673.1:g.66291208G>A	GRCh37
NC_000011.8:g.66047784G>A	NCBI36
NG_009093.1:g.18090G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.965G>A (BBS1) MANE Select	ENSP00000317469.7:p.Trp322Ter
ENST00000318312.11:c.965G>A (BBS1)	ENSP00000317469.7:p.Trp322Ter
ENST00000393994.4:c.724-2386G>A (BBS1)	ENSP00000377563.2:n.724-2386G>A
ENST00000419755.3:c.1076G>A	ENSP00000398526.3:p.Trp359Ter
ENST00000455748.6:c.674G>A (BBS1)	ENSP00000405764.2:p.Trp225Ter
ENST00000526760.5:c.*672G>A (BBS1)	ENSP00000432140.1:n.*672G>A
ENST00000526986.5:c.*22-2271C>T (ZDHHC24)	ENSP00000431321.1:n.*22-2271C>T
ENST00000527959.1:n.109G>A (BBS1)
ENST00000529766.5:n.972G>A (BBS1)
ENST00000529895.1:n.414G>A (BBS1)
ENST00000529955.5:n.936G>A (BBS1)
ENST00000532908.5:c.*625G>A (BBS1)	ENSP00000431866.1:n.*625G>A
ENST00000534073.5:c.*143+418C>T (ZDHHC24)	ENSP00000436503.1:n.*143+418C>T
ENST00000630659.2:c.*672G>A (BBS1)	ENSP00000486455.1:n.*672G>A
NM_024649.4:c.965G>A (BBS1)	NP_078925.3:p.Trp322Ter
XM_005273874.3:c.*22-2271C>T (ZDHHC24)	XP_005273931.1:n.*22-2271C>T
XR_949860.1:n.808+418C>T (ZDHHC24)
NM_001348571.1:c.*22-2271C>T (ZDHHC24)	NP_001335500.1:n.*22-2271C>T
XM_005273874.4:c.*22-2271C>T (ZDHHC24)	XP_005273931.1:n.*22-2271C>T
XR_001747823.2:n.862+418C>T (ZDHHC24)
XR_949860.3:n.933+418C>T (ZDHHC24)
NM_024649.5:c.965G>A (BBS1) MANE Select	NP_078925.3:p.Trp322Ter
NM_001348571.2:c.*22-2271C>T (ZDHHC24)	NP_001335500.1:n.*22-2271C>T