Canonical Allele Identifier: CA452820143
Gene: SERAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.158535906A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114874A>T , CM000668.2:g.158114874A>T GRCh38
NC_000006.11:g.158535906A>T , CM000668.1:g.158535906A>T GRCh37
NC_000006.10:g.158455894A>T NCBI36
NG_032889.1:g.58407T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.811T>A ENSP00000391168.2:n.811T>A
ENST00000607071.6:c.*1319T>A ENSP00000475855.1:n.*1319T>A
ENST00000642244.1:c.1509T>A ENSP00000493554.1:p.Pro503=
ENST00000642903.1:c.1599T>A ENSP00000493559.1:p.Pro533=
ENST00000644972.1:c.1599T>A ENSP00000496451.1:p.Pro533=
ENST00000645077.1:c.*1220T>A ENSP00000496113.1:n.*1220T>A
ENST00000645172.1:c.*1301T>A ENSP00000495367.1:n.*1301T>A
ENST00000646190.1:n.2930T>A
ENST00000646208.1:c.1335T>A ENSP00000493723.1:p.Pro445=
ENST00000646410.1:c.1470T>A ENSP00000494205.1:p.Pro490=
ENST00000646562.1:c.*1433T>A ENSP00000496087.1:n.*1433T>A
ENST00000647468.2:c.1599T>A MANE Select ENSP00000496731.1:p.Pro533=
ENST00000648111.1:c.*1287T>A ENSP00000497275.1:n.*1287T>A
ENST00000367101.5:c.*47T>A ENSP00000356068.1:n.*47T>A
ENST00000367104.7:c.1599T>A ENSP00000356071.3:p.Pro533=
ENST00000435180.5:c.324T>A ENSP00000391168.1:p.Pro108=
ENST00000606965.5:c.*160T>A ENSP00000475808.1:n.*160T>A
ENST00000607071.5:c.*1533T>A ENSP00000475855.1:n.*1533T>A
ENST00000607742.5:c.*2877T>A ENSP00000475523.1:n.*2877T>A
NM_032861.3:c.1599T>A NP_116250.3:p.Pro533=
NR_073096.1:n.1532T>A
XM_006715586.1:c.1389T>A XP_006715649.1:p.Pro463=
XM_011536196.1:c.1578T>A XP_011534498.1:p.Pro526=
XM_011536197.1:c.1485T>A XP_011534499.1:p.Pro495=
XM_011536198.1:c.1389T>A XP_011534500.1:p.Pro463=
XM_006715586.3:c.1389T>A XP_006715649.1:p.Pro463=
XM_011536196.3:c.1578T>A XP_011534498.1:p.Pro526=
XM_011536198.3:c.1389T>A XP_011534500.1:p.Pro463=
XM_024446573.1:c.1599T>A XP_024302341.1:p.Pro533=
XR_001743697.2:n.1630T>A
XR_942606.2:n.1681T>A
NM_032861.4:c.1599T>A MANE Select NP_116250.3:p.Pro533=
NR_073096.2:n.1514T>A