Canonical Allele Identifier: CA381422434

Gene: BBS1 ZDHHC24

Linked Data

• MyVariant Identifiers: chr11:g.66294132T>G (hg19) ; chr11:g.66526661T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66526661T>G , CM000673.2:g.66526661T>G	GRCh38
NC_000011.9:g.66294132T>G , CM000673.1:g.66294132T>G	GRCh37
NC_000011.8:g.66050708T>G	NCBI36
NG_009093.1:g.21014T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.1193T>G (BBS1) MANE Select	ENSP00000317469.7:p.Ile398Ser
ENST00000318312.11:c.1193T>G (BBS1)	ENSP00000317469.7:p.Ile398Ser
ENST00000393994.4:c.806T>G (BBS1)	ENSP00000377563.2:p.Ile269Ser
ENST00000419755.3:c.1304T>G	ENSP00000398526.3:p.Ile435Ser
ENST00000455748.6:c.902T>G (BBS1)	ENSP00000405764.2:p.Ile301Ser
ENST00000526760.5:c.*900T>G (BBS1)	ENSP00000432140.1:n.*900T>G
ENST00000526986.5:c.*21+275A>C (ZDHHC24)	ENSP00000431321.1:n.*21+275A>C
ENST00000527959.1:n.337T>G (BBS1)
ENST00000529766.5:n.1200T>G (BBS1)
ENST00000529955.5:n.1164T>G (BBS1)
ENST00000534073.5:c.*21+275A>C (ZDHHC24)	ENSP00000436503.1:n.*21+275A>C
ENST00000630659.2:c.*900T>G (BBS1)	ENSP00000486455.1:n.*900T>G
NM_024649.4:c.1193T>G (BBS1)	NP_078925.3:p.Ile398Ser
XM_005273874.3:c.*21+275A>C (ZDHHC24)	XP_005273931.1:n.*21+275A>C
XM_011544894.1:c.*21+275A>C (ZDHHC24)	XP_011543196.1:n.*21+275A>C
XM_011544895.1:c.560-2385A>C (ZDHHC24)	XP_011543197.1:n.560-2385A>C
XR_949860.1:n.686+275A>C (ZDHHC24)
NM_001348571.1:c.*21+275A>C (ZDHHC24)	NP_001335500.1:n.*21+275A>C
XM_005273874.4:c.*21+275A>C (ZDHHC24)	XP_005273931.1:n.*21+275A>C
XM_011544894.2:c.*21+275A>C (ZDHHC24)	XP_011543196.1:n.*21+275A>C
XR_001747823.2:n.741-2385A>C (ZDHHC24)
XR_949860.3:n.811+275A>C (ZDHHC24)
NM_024649.5:c.1193T>G (BBS1) MANE Select	NP_078925.3:p.Ile398Ser
NM_001348571.2:c.*21+275A>C (ZDHHC24)	NP_001335500.1:n.*21+275A>C