Canonical Allele Identifier: CA452822160
Gene: SERAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.158567881G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158146849G>A , CM000668.2:g.158146849G>A GRCh38
NC_000006.11:g.158567881G>A , CM000668.1:g.158567881G>A GRCh37
NC_000006.10:g.158487869G>A NCBI36
NG_032889.1:g.26432C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*254C>T ENSP00000475855.1:n.*254C>T
ENST00000642244.1:c.330C>T ENSP00000493554.1:p.Ser110=
ENST00000642903.1:c.420C>T ENSP00000493559.1:p.Ser140=
ENST00000644972.1:c.420C>T ENSP00000496451.1:p.Ser140=
ENST00000645077.1:c.*254C>T ENSP00000496113.1:n.*254C>T
ENST00000645172.1:c.*189+2016C>T ENSP00000495367.1:n.*189+2016C>T
ENST00000646190.1:n.1651C>T
ENST00000646208.1:c.156C>T ENSP00000493723.1:p.Ser52=
ENST00000646410.1:c.291C>T ENSP00000494205.1:p.Ser97=
ENST00000646562.1:c.*254C>T ENSP00000496087.1:n.*254C>T
ENST00000647468.2:c.420C>T MANE Select ENSP00000496731.1:p.Ser140=
ENST00000648111.1:c.*64C>T ENSP00000497275.1:n.*64C>T
ENST00000367101.5:c.420C>T ENSP00000356068.1:p.Ser140=
ENST00000367104.7:c.420C>T ENSP00000356071.3:p.Ser140=
ENST00000606965.5:c.420C>T ENSP00000475808.1:p.Ser140=
ENST00000607000.1:c.420C>T ENSP00000475788.1:p.Ser140=
ENST00000607071.5:c.*254C>T ENSP00000475855.1:n.*254C>T
ENST00000607742.5:c.*254C>T ENSP00000475523.1:n.*254C>T
NM_032861.3:c.420C>T NP_116250.3:p.Ser140=
NR_073096.1:n.562C>T
XM_006715586.1:c.210C>T XP_006715649.1:p.Ser70=
XM_011536196.1:c.399C>T XP_011534498.1:p.Ser133=
XM_011536197.1:c.420C>T XP_011534499.1:p.Ser140=
XM_011536198.1:c.210C>T XP_011534500.1:p.Ser70=
XR_942606.1:n.421C>T
XM_006715586.3:c.210C>T XP_006715649.1:p.Ser70=
XM_011536196.3:c.399C>T XP_011534498.1:p.Ser133=
XM_011536198.3:c.210C>T XP_011534500.1:p.Ser70=
XM_024446573.1:c.420C>T XP_024302341.1:p.Ser140=
XR_001743697.2:n.501C>T
XR_942606.2:n.552C>T
NM_032861.4:c.420C>T MANE Select NP_116250.3:p.Ser140=
NR_073096.2:n.544C>T