Canonical Allele Identifier: CA381462606

Gene: BBS1 ZDHHC24

Linked Data

• MyVariant Identifiers: chr11:g.66291313T>G (hg19) ; chr11:g.66523842T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66523842T>G , CM000673.2:g.66523842T>G	GRCh38
NC_000011.9:g.66291313T>G , CM000673.1:g.66291313T>G	GRCh37
NC_000011.8:g.66047889T>G	NCBI36
NG_009093.1:g.18195T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.1070T>G (BBS1) MANE Select	ENSP00000317469.7:p.Ile357Ser
ENST00000318312.11:c.1070T>G (BBS1)	ENSP00000317469.7:p.Ile357Ser
ENST00000393994.4:c.724-2281T>G (BBS1)	ENSP00000377563.2:n.724-2281T>G
ENST00000419755.3:c.1181T>G	ENSP00000398526.3:p.Ile394Ser
ENST00000455748.6:c.779T>G (BBS1)	ENSP00000405764.2:p.Ile260Ser
ENST00000526760.5:c.*777T>G (BBS1)	ENSP00000432140.1:n.*777T>G
ENST00000526986.5:c.*22-2376A>C (ZDHHC24)	ENSP00000431321.1:n.*22-2376A>C
ENST00000527959.1:n.214T>G (BBS1)
ENST00000529766.5:n.1077T>G (BBS1)
ENST00000529895.1:n.519T>G (BBS1)
ENST00000529955.5:n.1041T>G (BBS1)
ENST00000532908.5:c.*730T>G (BBS1)	ENSP00000431866.1:n.*730T>G
ENST00000534073.5:c.*143+313A>C (ZDHHC24)	ENSP00000436503.1:n.*143+313A>C
ENST00000630659.2:c.*777T>G (BBS1)	ENSP00000486455.1:n.*777T>G
NM_024649.4:c.1070T>G (BBS1)	NP_078925.3:p.Ile357Ser
XM_005273874.3:c.*22-2376A>C (ZDHHC24)	XP_005273931.1:n.*22-2376A>C
XR_949860.1:n.808+313A>C (ZDHHC24)
NM_001348571.1:c.*22-2376A>C (ZDHHC24)	NP_001335500.1:n.*22-2376A>C
XM_005273874.4:c.*22-2376A>C (ZDHHC24)	XP_005273931.1:n.*22-2376A>C
XR_001747823.2:n.862+313A>C (ZDHHC24)
XR_949860.3:n.933+313A>C (ZDHHC24)
NM_024649.5:c.1070T>G (BBS1) MANE Select	NP_078925.3:p.Ile357Ser
NM_001348571.2:c.*22-2376A>C (ZDHHC24)	NP_001335500.1:n.*22-2376A>C