Canonical Allele Identifier: CA381462575
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66523836T>A , CM000673.2:g.66523836T>A GRCh38
NC_000011.9:g.66291307T>A , CM000673.1:g.66291307T>A GRCh37
NC_000011.8:g.66047883T>A NCBI36
NG_009093.1:g.18189T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1064T>A (BBS1) MANE Select ENSP00000317469.7:p.Val355Asp
ENST00000318312.11:c.1064T>A (BBS1) ENSP00000317469.7:p.Val355Asp
ENST00000393994.4:c.724-2287T>A (BBS1) ENSP00000377563.2:n.724-2287T>A
ENST00000419755.3:c.1175T>A ENSP00000398526.3:p.Val392Asp
ENST00000455748.6:c.773T>A (BBS1) ENSP00000405764.2:p.Val258Asp
ENST00000526760.5:c.*771T>A (BBS1) ENSP00000432140.1:n.*771T>A
ENST00000526986.5:c.*22-2370A>T (ZDHHC24) ENSP00000431321.1:n.*22-2370A>T
ENST00000527959.1:n.208T>A (BBS1)
ENST00000529766.5:n.1071T>A (BBS1)
ENST00000529895.1:n.513T>A (BBS1)
ENST00000529955.5:n.1035T>A (BBS1)
ENST00000532908.5:c.*724T>A (BBS1) ENSP00000431866.1:n.*724T>A
ENST00000534073.5:c.*143+319A>T (ZDHHC24) ENSP00000436503.1:n.*143+319A>T
ENST00000630659.2:c.*771T>A (BBS1) ENSP00000486455.1:n.*771T>A
NM_024649.4:c.1064T>A (BBS1) NP_078925.3:p.Val355Asp
XM_005273874.3:c.*22-2370A>T (ZDHHC24) XP_005273931.1:n.*22-2370A>T
XR_949860.1:n.808+319A>T (ZDHHC24)
NM_001348571.1:c.*22-2370A>T (ZDHHC24) NP_001335500.1:n.*22-2370A>T
XM_005273874.4:c.*22-2370A>T (ZDHHC24) XP_005273931.1:n.*22-2370A>T
XR_001747823.2:n.862+319A>T (ZDHHC24)
XR_949860.3:n.933+319A>T (ZDHHC24)
NM_024649.5:c.1064T>A (BBS1) MANE Select NP_078925.3:p.Val355Asp
NM_001348571.2:c.*22-2370A>T (ZDHHC24) NP_001335500.1:n.*22-2370A>T