Canonical Allele Identifier: CA2724299794
Gene: BBS1 HGNC NCBI
ZDHHC24 HGNC NCBI

Linked Data

dbSNP Id: rs1856532603

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66526869G>A , CM000673.2:g.66526869G>A GRCh38
NC_000011.9:g.66294340G>A , CM000673.1:g.66294340G>A GRCh37
NC_000011.8:g.66050916G>A NCBI36
NG_009093.1:g.21222G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.1339+62G>A (BBS1) MANE Select ENSP00000317469.7:n.1339+62G>A
ENST00000318312.11:c.1339+62G>A (BBS1) ENSP00000317469.7:n.1339+62G>A
ENST00000393994.4:c.952+62G>A (BBS1) ENSP00000377563.2:n.952+62G>A
ENST00000419755.3:c.1450+62G>A ENSP00000398526.3:n.1450+62G>A
ENST00000455748.6:c.1048+62G>A (BBS1) ENSP00000405764.2:n.1048+62G>A
ENST00000526760.5:c.*1046+62G>A (BBS1) ENSP00000432140.1:n.*1046+62G>A
ENST00000526986.5:c.*21+67C>T (ZDHHC24) ENSP00000431321.1:n.*21+67C>T
ENST00000527959.1:n.545G>A (BBS1)
ENST00000529766.5:n.1408G>A (BBS1)
ENST00000529955.5:n.1310+62G>A (BBS1)
ENST00000534073.5:c.*21+67C>T (ZDHHC24) ENSP00000436503.1:n.*21+67C>T
ENST00000630659.2:c.*1046+62G>A (BBS1) ENSP00000486455.1:n.*1046+62G>A
NM_024649.4:c.1339+62G>A (BBS1) NP_078925.3:n.1339+62G>A
XM_005273874.3:c.*21+67C>T (ZDHHC24) XP_005273931.1:n.*21+67C>T
XM_011544894.1:c.*21+67C>T (ZDHHC24) XP_011543196.1:n.*21+67C>T
XM_011544895.1:c.560-2593C>T (ZDHHC24) XP_011543197.1:n.560-2593C>T
XR_949860.1:n.686+67C>T (ZDHHC24)
NM_001348571.1:c.*21+67C>T (ZDHHC24) NP_001335500.1:n.*21+67C>T
XM_005273874.4:c.*21+67C>T (ZDHHC24) XP_005273931.1:n.*21+67C>T
XM_011544894.2:c.*21+67C>T (ZDHHC24) XP_011543196.1:n.*21+67C>T
XR_001747823.2:n.741-2593C>T (ZDHHC24)
XR_949860.3:n.811+67C>T (ZDHHC24)
NM_024649.5:c.1339+62G>A (BBS1) MANE Select NP_078925.3:n.1339+62G>A
NM_001348571.2:c.*21+67C>T (ZDHHC24) NP_001335500.1:n.*21+67C>T