Canonical Allele Identifier: CA475492065
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.66291215G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523744G>T , CM000673.2:g.66523744G>T GRCh38
NC_000011.9:g.66291215G>T , CM000673.1:g.66291215G>T GRCh37
NC_000011.8:g.66047791G>T NCBI36
NG_009093.1:g.18097G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.972G>T (BBS1) MANE Select ENSP00000317469.7:p.Val324=
ENST00000318312.11:c.972G>T (BBS1) ENSP00000317469.7:p.Val324=
ENST00000393994.4:c.724-2379G>T (BBS1) ENSP00000377563.2:n.724-2379G>T
ENST00000419755.3:c.1083G>T ENSP00000398526.3:p.Val361=
ENST00000455748.6:c.681G>T (BBS1) ENSP00000405764.2:p.Val227=
ENST00000526760.5:c.*679G>T (BBS1) ENSP00000432140.1:n.*679G>T
ENST00000526986.5:c.*22-2278C>A (ZDHHC24) ENSP00000431321.1:n.*22-2278C>A
ENST00000527959.1:n.116G>T (BBS1)
ENST00000529766.5:n.979G>T (BBS1)
ENST00000529895.1:n.421G>T (BBS1)
ENST00000529955.5:n.943G>T (BBS1)
ENST00000532908.5:c.*632G>T (BBS1) ENSP00000431866.1:n.*632G>T
ENST00000534073.5:c.*143+411C>A (ZDHHC24) ENSP00000436503.1:n.*143+411C>A
ENST00000630659.2:c.*679G>T (BBS1) ENSP00000486455.1:n.*679G>T
NM_024649.4:c.972G>T (BBS1) NP_078925.3:p.Val324=
XM_005273874.3:c.*22-2278C>A (ZDHHC24) XP_005273931.1:n.*22-2278C>A
XR_949860.1:n.808+411C>A (ZDHHC24)
NM_001348571.1:c.*22-2278C>A (ZDHHC24) NP_001335500.1:n.*22-2278C>A
XM_005273874.4:c.*22-2278C>A (ZDHHC24) XP_005273931.1:n.*22-2278C>A
XR_001747823.2:n.862+411C>A (ZDHHC24)
XR_949860.3:n.933+411C>A (ZDHHC24)
NM_024649.5:c.972G>T (BBS1) MANE Select NP_078925.3:p.Val324=
NM_001348571.2:c.*22-2278C>A (ZDHHC24) NP_001335500.1:n.*22-2278C>A