Canonical Allele Identifier: CA475492069
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.66291227A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523756A>C , CM000673.2:g.66523756A>C GRCh38
NC_000011.9:g.66291227A>C , CM000673.1:g.66291227A>C GRCh37
NC_000011.8:g.66047803A>C NCBI36
NG_009093.1:g.18109A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.984A>C (BBS1) MANE Select ENSP00000317469.7:p.Ala328=
ENST00000318312.11:c.984A>C (BBS1) ENSP00000317469.7:p.Ala328=
ENST00000393994.4:c.724-2367A>C (BBS1) ENSP00000377563.2:n.724-2367A>C
ENST00000419755.3:c.1095A>C ENSP00000398526.3:p.Ala365=
ENST00000455748.6:c.693A>C (BBS1) ENSP00000405764.2:p.Ala231=
ENST00000526760.5:c.*691A>C (BBS1) ENSP00000432140.1:n.*691A>C
ENST00000526986.5:c.*22-2290T>G (ZDHHC24) ENSP00000431321.1:n.*22-2290T>G
ENST00000527959.1:n.128A>C (BBS1)
ENST00000529766.5:n.991A>C (BBS1)
ENST00000529895.1:n.433A>C (BBS1)
ENST00000529955.5:n.955A>C (BBS1)
ENST00000532908.5:c.*644A>C (BBS1) ENSP00000431866.1:n.*644A>C
ENST00000534073.5:c.*143+399T>G (ZDHHC24) ENSP00000436503.1:n.*143+399T>G
ENST00000630659.2:c.*691A>C (BBS1) ENSP00000486455.1:n.*691A>C
NM_024649.4:c.984A>C (BBS1) NP_078925.3:p.Ala328=
XM_005273874.3:c.*22-2290T>G (ZDHHC24) XP_005273931.1:n.*22-2290T>G
XR_949860.1:n.808+399T>G (ZDHHC24)
NM_001348571.1:c.*22-2290T>G (ZDHHC24) NP_001335500.1:n.*22-2290T>G
XM_005273874.4:c.*22-2290T>G (ZDHHC24) XP_005273931.1:n.*22-2290T>G
XR_001747823.2:n.862+399T>G (ZDHHC24)
XR_949860.3:n.933+399T>G (ZDHHC24)
NM_024649.5:c.984A>C (BBS1) MANE Select NP_078925.3:p.Ala328=
NM_001348571.2:c.*22-2290T>G (ZDHHC24) NP_001335500.1:n.*22-2290T>G