Canonical Allele Identifier: CA452820188
Gene: SERAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.158535983G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114951G>A , CM000668.2:g.158114951G>A GRCh38
NC_000006.11:g.158535983G>A , CM000668.1:g.158535983G>A GRCh37
NC_000006.10:g.158455971G>A NCBI36
NG_032889.1:g.58330C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.734C>T ENSP00000391168.2:n.734C>T
ENST00000607071.6:c.*1242C>T ENSP00000475855.1:n.*1242C>T
ENST00000642244.1:c.1432C>T ENSP00000493554.1:p.Leu478=
ENST00000642903.1:c.1522C>T ENSP00000493559.1:p.Leu508=
ENST00000644972.1:c.1522C>T ENSP00000496451.1:p.Leu508=
ENST00000645077.1:c.*1143C>T ENSP00000496113.1:n.*1143C>T
ENST00000645172.1:c.*1224C>T ENSP00000495367.1:n.*1224C>T
ENST00000646190.1:n.2853C>T
ENST00000646208.1:c.1258C>T ENSP00000493723.1:p.Leu420=
ENST00000646410.1:c.1393C>T ENSP00000494205.1:p.Leu465=
ENST00000646562.1:c.*1356C>T ENSP00000496087.1:n.*1356C>T
ENST00000647468.2:c.1522C>T MANE Select ENSP00000496731.1:p.Leu508=
ENST00000648111.1:c.*1210C>T ENSP00000497275.1:n.*1210C>T
ENST00000367101.5:c.1566C>T ENSP00000356068.1:p.Cys522=
ENST00000367104.7:c.1522C>T ENSP00000356071.3:p.Leu508=
ENST00000435180.5:c.247C>T ENSP00000391168.1:p.Leu83=
ENST00000606965.5:c.*83C>T ENSP00000475808.1:n.*83C>T
ENST00000607071.5:c.*1456C>T ENSP00000475855.1:n.*1456C>T
ENST00000607742.5:c.*2800C>T ENSP00000475523.1:n.*2800C>T
NM_032861.3:c.1522C>T NP_116250.3:p.Leu508=
NR_073096.1:n.1455C>T
XM_006715586.1:c.1312C>T XP_006715649.1:p.Leu438=
XM_011536196.1:c.1501C>T XP_011534498.1:p.Leu501=
XM_011536197.1:c.1408C>T XP_011534499.1:p.Leu470=
XM_011536198.1:c.1312C>T XP_011534500.1:p.Leu438=
XM_006715586.3:c.1312C>T XP_006715649.1:p.Leu438=
XM_011536196.3:c.1501C>T XP_011534498.1:p.Leu501=
XM_011536198.3:c.1312C>T XP_011534500.1:p.Leu438=
XM_024446573.1:c.1522C>T XP_024302341.1:p.Leu508=
XR_001743697.2:n.1553C>T
XR_942606.2:n.1604C>T
NM_032861.4:c.1522C>T MANE Select NP_116250.3:p.Leu508=
NR_073096.2:n.1437C>T