Canonical Allele Identifier: CA366254995
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114843C>A , CM000668.2:g.158114843C>A GRCh38
NC_000006.11:g.158535875C>A , CM000668.1:g.158535875C>A GRCh37
NC_000006.10:g.158455863C>A NCBI36
NG_032889.1:g.58438G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.842G>T ENSP00000391168.2:n.842G>T
ENST00000607071.6:c.*1350G>T ENSP00000475855.1:n.*1350G>T
ENST00000642244.1:c.1540G>T ENSP00000493554.1:p.Val514Phe
ENST00000642903.1:c.1630G>T ENSP00000493559.1:p.Val544Phe
ENST00000644972.1:c.1630G>T ENSP00000496451.1:p.Val544Phe
ENST00000645077.1:c.*1251G>T ENSP00000496113.1:n.*1251G>T
ENST00000645172.1:c.*1332G>T ENSP00000495367.1:n.*1332G>T
ENST00000646190.1:n.2961G>T
ENST00000646208.1:c.1366G>T ENSP00000493723.1:p.Val456Phe
ENST00000646410.1:c.1501G>T ENSP00000494205.1:p.Val501Phe
ENST00000646562.1:c.*1464G>T ENSP00000496087.1:n.*1464G>T
ENST00000647468.2:c.1630G>T MANE Select ENSP00000496731.1:p.Val544Phe
ENST00000648111.1:c.*1318G>T ENSP00000497275.1:n.*1318G>T
ENST00000367101.5:c.*78G>T ENSP00000356068.1:n.*78G>T
ENST00000367104.7:c.1630G>T ENSP00000356071.3:p.Val544Phe
ENST00000435180.5:c.355G>T ENSP00000391168.1:p.Val119Phe
ENST00000606965.5:c.*191G>T ENSP00000475808.1:n.*191G>T
ENST00000607071.5:c.*1564G>T ENSP00000475855.1:n.*1564G>T
ENST00000607742.5:c.*2908G>T ENSP00000475523.1:n.*2908G>T
NM_032861.3:c.1630G>T NP_116250.3:p.Val544Phe
NR_073096.1:n.1563G>T
XM_006715586.1:c.1420G>T XP_006715649.1:p.Val474Phe
XM_011536196.1:c.1609G>T XP_011534498.1:p.Val537Phe
XM_011536197.1:c.1516G>T XP_011534499.1:p.Val506Phe
XM_011536198.1:c.1420G>T XP_011534500.1:p.Val474Phe
XM_006715586.3:c.1420G>T XP_006715649.1:p.Val474Phe
XM_011536196.3:c.1609G>T XP_011534498.1:p.Val537Phe
XM_011536198.3:c.1420G>T XP_011534500.1:p.Val474Phe
XM_024446573.1:c.1630G>T XP_024302341.1:p.Val544Phe
XR_001743697.2:n.1661G>T
XR_942606.2:n.1712G>T
NM_032861.4:c.1630G>T MANE Select NP_116250.3:p.Val544Phe
NR_073096.2:n.1545G>T