Canonical Allele Identifier: CA366255305

Gene: SERAC1

Linked Data

• dbSNP Id: rs1784249017
• MyVariant Identifiers: chr6:g.158536003C>A (hg19) ; chr6:g.158114971C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114971C>A , CM000668.2:g.158114971C>A	GRCh38
NC_000006.11:g.158536003C>A , CM000668.1:g.158536003C>A	GRCh37
NC_000006.10:g.158455991C>A	NCBI36
NG_032889.1:g.58310G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.714G>T	ENSP00000391168.2:n.714G>T
ENST00000607071.6:c.*1222G>T	ENSP00000475855.1:n.*1222G>T
ENST00000642244.1:c.1412G>T	ENSP00000493554.1:p.Gly471Val
ENST00000642903.1:c.1502G>T	ENSP00000493559.1:p.Gly501Val
ENST00000644972.1:c.1502G>T	ENSP00000496451.1:p.Gly501Val
ENST00000645077.1:c.*1123G>T	ENSP00000496113.1:n.*1123G>T
ENST00000645172.1:c.*1204G>T	ENSP00000495367.1:n.*1204G>T
ENST00000646190.1:n.2833G>T
ENST00000646208.1:c.1238G>T	ENSP00000493723.1:p.Gly413Val
ENST00000646410.1:c.1373G>T	ENSP00000494205.1:p.Gly458Val
ENST00000646562.1:c.*1336G>T	ENSP00000496087.1:n.*1336G>T
ENST00000647468.2:c.1502G>T MANE Select	ENSP00000496731.1:p.Gly501Val
ENST00000648111.1:c.*1190G>T	ENSP00000497275.1:n.*1190G>T
ENST00000367101.5:c.1546G>T	ENSP00000356068.1:p.Val516Phe
ENST00000367104.7:c.1502G>T	ENSP00000356071.3:p.Gly501Val
ENST00000435180.5:c.227G>T	ENSP00000391168.1:p.Gly76Val
ENST00000606965.5:c.*63G>T	ENSP00000475808.1:n.*63G>T
ENST00000607071.5:c.*1436G>T	ENSP00000475855.1:n.*1436G>T
ENST00000607742.5:c.*2780G>T	ENSP00000475523.1:n.*2780G>T
NM_032861.3:c.1502G>T	NP_116250.3:p.Gly501Val
NR_073096.1:n.1435G>T
XM_006715586.1:c.1292G>T	XP_006715649.1:p.Gly431Val
XM_011536196.1:c.1481G>T	XP_011534498.1:p.Gly494Val
XM_011536197.1:c.1388G>T	XP_011534499.1:p.Gly463Val
XM_011536198.1:c.1292G>T	XP_011534500.1:p.Gly431Val
XM_006715586.3:c.1292G>T	XP_006715649.1:p.Gly431Val
XM_011536196.3:c.1481G>T	XP_011534498.1:p.Gly494Val
XM_011536198.3:c.1292G>T	XP_011534500.1:p.Gly431Val
XM_024446573.1:c.1502G>T	XP_024302341.1:p.Gly501Val
XR_001743697.2:n.1533G>T
XR_942606.2:n.1584G>T
NM_032861.4:c.1502G>T MANE Select	NP_116250.3:p.Gly501Val
NR_073096.2:n.1417G>T