Canonical Allele Identifier: CA267611
Gene: SERAC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 120184
ClinVar RCV Id: RCV000106307
dbSNP Id: rs529232938

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158150516G>A , CM000668.2:g.158150516G>A GRCh38
NC_000006.11:g.158571548G>A , CM000668.1:g.158571548G>A GRCh37
NC_000006.10:g.158491536G>A NCBI36
NG_032889.1:g.22765C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000607071.6:c.*36C>T ENSP00000475855.1:n.*36C>T
ENST00000642244.1:c.202C>T ENSP00000493554.1:p.Arg68Ter
ENST00000642903.1:c.202C>T ENSP00000493559.1:p.Arg68Ter
ENST00000643093.1:n.252C>T
ENST00000644972.1:c.202C>T ENSP00000496451.1:p.Arg68Ter
ENST00000645077.1:c.*36C>T ENSP00000496113.1:n.*36C>T
ENST00000645172.1:c.*36C>T ENSP00000495367.1:n.*36C>T
ENST00000646190.1:n.1433C>T
ENST00000646208.1:c.92-3603C>T ENSP00000493723.1:n.92-3603C>T
ENST00000646410.1:c.163C>T ENSP00000494205.1:p.Arg55Ter
ENST00000646562.1:c.*36C>T ENSP00000496087.1:n.*36C>T
ENST00000647468.2:c.202C>T MANE Select ENSP00000496731.1:p.Arg68Ter
ENST00000648111.1:c.176C>T ENSP00000497275.1:p.Thr59Met
ENST00000367101.5:c.202C>T ENSP00000356068.1:p.Arg68Ter
ENST00000367104.7:c.202C>T ENSP00000356071.3:p.Arg68Ter
ENST00000606965.5:c.202C>T ENSP00000475808.1:p.Arg68Ter
ENST00000607000.1:c.202C>T ENSP00000475788.1:p.Arg68Ter
ENST00000607071.5:c.*36C>T ENSP00000475855.1:n.*36C>T
ENST00000607742.5:c.*36C>T ENSP00000475523.1:n.*36C>T
NM_032861.3:c.202C>T NP_116250.3:p.Arg68Ter
NR_073096.1:n.344C>T
XM_006715586.1:c.-9C>T XP_006715649.1:n.-9C>T
XM_011536196.1:c.181C>T XP_011534498.1:p.Arg61Ter
XM_011536197.1:c.202C>T XP_011534499.1:p.Arg68Ter
XM_011536198.1:c.-9C>T XP_011534500.1:n.-9C>T
XR_942606.1:n.203C>T
XM_006715586.3:c.-9C>T XP_006715649.1:n.-9C>T
XM_011536196.3:c.181C>T XP_011534498.1:p.Arg61Ter
XM_011536198.3:c.-9C>T XP_011534500.1:n.-9C>T
XM_024446573.1:c.202C>T XP_024302341.1:p.Arg68Ter
XR_001743697.2:n.283C>T
XR_942606.2:n.334C>T
NM_032861.4:c.202C>T MANE Select NP_116250.3:p.Arg68Ter
NR_073096.2:n.326C>T