Canonical Allele Identifier: CA366255215

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535970G>C (hg19) ; chr6:g.158114938G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114938G>C , CM000668.2:g.158114938G>C	GRCh38
NC_000006.11:g.158535970G>C , CM000668.1:g.158535970G>C	GRCh37
NC_000006.10:g.158455958G>C	NCBI36
NG_032889.1:g.58343C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.747C>G	ENSP00000391168.2:n.747C>G
ENST00000607071.6:c.*1255C>G	ENSP00000475855.1:n.*1255C>G
ENST00000642244.1:c.1445C>G	ENSP00000493554.1:p.Ser482Cys
ENST00000642903.1:c.1535C>G	ENSP00000493559.1:p.Ser512Cys
ENST00000644972.1:c.1535C>G	ENSP00000496451.1:p.Ser512Cys
ENST00000645077.1:c.*1156C>G	ENSP00000496113.1:n.*1156C>G
ENST00000645172.1:c.*1237C>G	ENSP00000495367.1:n.*1237C>G
ENST00000646190.1:n.2866C>G
ENST00000646208.1:c.1271C>G	ENSP00000493723.1:p.Ser424Cys
ENST00000646410.1:c.1406C>G	ENSP00000494205.1:p.Ser469Cys
ENST00000646562.1:c.*1369C>G	ENSP00000496087.1:n.*1369C>G
ENST00000647468.2:c.1535C>G MANE Select	ENSP00000496731.1:p.Ser512Cys
ENST00000648111.1:c.*1223C>G	ENSP00000497275.1:n.*1223C>G
ENST00000367101.5:c.1579C>G	ENSP00000356068.1:p.Leu527Val
ENST00000367104.7:c.1535C>G	ENSP00000356071.3:p.Ser512Cys
ENST00000435180.5:c.260C>G	ENSP00000391168.1:p.Ser87Cys
ENST00000606965.5:c.*96C>G	ENSP00000475808.1:n.*96C>G
ENST00000607071.5:c.*1469C>G	ENSP00000475855.1:n.*1469C>G
ENST00000607742.5:c.*2813C>G	ENSP00000475523.1:n.*2813C>G
NM_032861.3:c.1535C>G	NP_116250.3:p.Ser512Cys
NR_073096.1:n.1468C>G
XM_006715586.1:c.1325C>G	XP_006715649.1:p.Ser442Cys
XM_011536196.1:c.1514C>G	XP_011534498.1:p.Ser505Cys
XM_011536197.1:c.1421C>G	XP_011534499.1:p.Ser474Cys
XM_011536198.1:c.1325C>G	XP_011534500.1:p.Ser442Cys
XM_006715586.3:c.1325C>G	XP_006715649.1:p.Ser442Cys
XM_011536196.3:c.1514C>G	XP_011534498.1:p.Ser505Cys
XM_011536198.3:c.1325C>G	XP_011534500.1:p.Ser442Cys
XM_024446573.1:c.1535C>G	XP_024302341.1:p.Ser512Cys
XR_001743697.2:n.1566C>G
XR_942606.2:n.1617C>G
NM_032861.4:c.1535C>G MANE Select	NP_116250.3:p.Ser512Cys
NR_073096.2:n.1450C>G