Canonical Allele Identifier: CA452820180
Gene: SERAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.158535945A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114913A>C , CM000668.2:g.158114913A>C GRCh38
NC_000006.11:g.158535945A>C , CM000668.1:g.158535945A>C GRCh37
NC_000006.10:g.158455933A>C NCBI36
NG_032889.1:g.58368T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.772T>G ENSP00000391168.2:n.772T>G
ENST00000607071.6:c.*1280T>G ENSP00000475855.1:n.*1280T>G
ENST00000642244.1:c.1470T>G ENSP00000493554.1:p.Val490=
ENST00000642903.1:c.1560T>G ENSP00000493559.1:p.Val520=
ENST00000644972.1:c.1560T>G ENSP00000496451.1:p.Val520=
ENST00000645077.1:c.*1181T>G ENSP00000496113.1:n.*1181T>G
ENST00000645172.1:c.*1262T>G ENSP00000495367.1:n.*1262T>G
ENST00000646190.1:n.2891T>G
ENST00000646208.1:c.1296T>G ENSP00000493723.1:p.Val432=
ENST00000646410.1:c.1431T>G ENSP00000494205.1:p.Val477=
ENST00000646562.1:c.*1394T>G ENSP00000496087.1:n.*1394T>G
ENST00000647468.2:c.1560T>G MANE Select ENSP00000496731.1:p.Val520=
ENST00000648111.1:c.*1248T>G ENSP00000497275.1:n.*1248T>G
ENST00000367101.5:c.*8T>G ENSP00000356068.1:n.*8T>G
ENST00000367104.7:c.1560T>G ENSP00000356071.3:p.Val520=
ENST00000435180.5:c.285T>G ENSP00000391168.1:p.Val95=
ENST00000606965.5:c.*121T>G ENSP00000475808.1:n.*121T>G
ENST00000607071.5:c.*1494T>G ENSP00000475855.1:n.*1494T>G
ENST00000607742.5:c.*2838T>G ENSP00000475523.1:n.*2838T>G
NM_032861.3:c.1560T>G NP_116250.3:p.Val520=
NR_073096.1:n.1493T>G
XM_006715586.1:c.1350T>G XP_006715649.1:p.Val450=
XM_011536196.1:c.1539T>G XP_011534498.1:p.Val513=
XM_011536197.1:c.1446T>G XP_011534499.1:p.Val482=
XM_011536198.1:c.1350T>G XP_011534500.1:p.Val450=
XM_006715586.3:c.1350T>G XP_006715649.1:p.Val450=
XM_011536196.3:c.1539T>G XP_011534498.1:p.Val513=
XM_011536198.3:c.1350T>G XP_011534500.1:p.Val450=
XM_024446573.1:c.1560T>G XP_024302341.1:p.Val520=
XR_001743697.2:n.1591T>G
XR_942606.2:n.1642T>G
NM_032861.4:c.1560T>G MANE Select NP_116250.3:p.Val520=
NR_073096.2:n.1475T>G