Canonical Allele Identifier: CA366255189
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114928T>G , CM000668.2:g.158114928T>G GRCh38
NC_000006.11:g.158535960T>G , CM000668.1:g.158535960T>G GRCh37
NC_000006.10:g.158455948T>G NCBI36
NG_032889.1:g.58353A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.757A>C ENSP00000391168.2:n.757A>C
ENST00000607071.6:c.*1265A>C ENSP00000475855.1:n.*1265A>C
ENST00000642244.1:c.1455A>C ENSP00000493554.1:p.Pro485=
ENST00000642903.1:c.1545A>C ENSP00000493559.1:p.Pro515=
ENST00000644972.1:c.1545A>C ENSP00000496451.1:p.Pro515=
ENST00000645077.1:c.*1166A>C ENSP00000496113.1:n.*1166A>C
ENST00000645172.1:c.*1247A>C ENSP00000495367.1:n.*1247A>C
ENST00000646190.1:n.2876A>C
ENST00000646208.1:c.1281A>C ENSP00000493723.1:p.Pro427=
ENST00000646410.1:c.1416A>C ENSP00000494205.1:p.Pro472=
ENST00000646562.1:c.*1379A>C ENSP00000496087.1:n.*1379A>C
ENST00000647468.2:c.1545A>C MANE Select ENSP00000496731.1:p.Pro515=
ENST00000648111.1:c.*1233A>C ENSP00000497275.1:n.*1233A>C
ENST00000367101.5:c.1589A>C ENSP00000356068.1:p.Gln530Pro
ENST00000367104.7:c.1545A>C ENSP00000356071.3:p.Pro515=
ENST00000435180.5:c.270A>C ENSP00000391168.1:p.Pro90=
ENST00000606965.5:c.*106A>C ENSP00000475808.1:n.*106A>C
ENST00000607071.5:c.*1479A>C ENSP00000475855.1:n.*1479A>C
ENST00000607742.5:c.*2823A>C ENSP00000475523.1:n.*2823A>C
NM_032861.3:c.1545A>C NP_116250.3:p.Pro515=
NR_073096.1:n.1478A>C
XM_006715586.1:c.1335A>C XP_006715649.1:p.Pro445=
XM_011536196.1:c.1524A>C XP_011534498.1:p.Pro508=
XM_011536197.1:c.1431A>C XP_011534499.1:p.Pro477=
XM_011536198.1:c.1335A>C XP_011534500.1:p.Pro445=
XM_006715586.3:c.1335A>C XP_006715649.1:p.Pro445=
XM_011536196.3:c.1524A>C XP_011534498.1:p.Pro508=
XM_011536198.3:c.1335A>C XP_011534500.1:p.Pro445=
XM_024446573.1:c.1545A>C XP_024302341.1:p.Pro515=
XR_001743697.2:n.1576A>C
XR_942606.2:n.1627A>C
NM_032861.4:c.1545A>C MANE Select NP_116250.3:p.Pro515=
NR_073096.2:n.1460A>C