Canonical Allele Identifier: CA1675959479

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114935G= , CM000668.2:g.158114935G=	GRCh38
NC_000006.11:g.158535967G= , CM000668.1:g.158535967G=	GRCh37
NC_000006.10:g.158455955G=	NCBI36
NG_032889.1:g.58346C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.750C=	ENSP00000391168.2:n.750C=
ENST00000607071.6:c.*1258C=	ENSP00000475855.1:n.*1258C=
ENST00000642244.1:c.1448C=	ENSP00000493554.1:p.Thr483=
ENST00000642903.1:c.1538C=	ENSP00000493559.1:p.Thr513=
ENST00000644972.1:c.1538C=	ENSP00000496451.1:p.Thr513=
ENST00000645077.1:c.*1159C=	ENSP00000496113.1:n.*1159C=
ENST00000645172.1:c.*1240C=	ENSP00000495367.1:n.*1240C=
ENST00000646190.1:n.2869C=
ENST00000646208.1:c.1274C=	ENSP00000493723.1:p.Thr425=
ENST00000646410.1:c.1409C=	ENSP00000494205.1:p.Thr470=
ENST00000646562.1:c.*1372C=	ENSP00000496087.1:n.*1372C=
ENST00000647468.2:c.1538C= MANE Select	ENSP00000496731.1:p.Thr513=
ENST00000648111.1:c.*1226C=	ENSP00000497275.1:n.*1226C=
ENST00000367101.5:c.1582C=	ENSP00000356068.1:p.Arg528=
ENST00000367104.7:c.1538C=	ENSP00000356071.3:p.Thr513=
ENST00000435180.5:c.263C=	ENSP00000391168.1:p.Thr88=
ENST00000606965.5:c.*99C=	ENSP00000475808.1:n.*99C=
ENST00000607071.5:c.*1472C=	ENSP00000475855.1:n.*1472C=
ENST00000607742.5:c.*2816C=	ENSP00000475523.1:n.*2816C=
NM_032861.3:c.1538C=	NP_116250.3:p.Thr513=
NR_073096.1:n.1471C=
XM_006715586.1:c.1328C=	XP_006715649.1:p.Thr443=
XM_011536196.1:c.1517C=	XP_011534498.1:p.Thr506=
XM_011536197.1:c.1424C=	XP_011534499.1:p.Thr475=
XM_011536198.1:c.1328C=	XP_011534500.1:p.Thr443=
XM_006715586.3:c.1328C=	XP_006715649.1:p.Thr443=
XM_011536196.3:c.1517C=	XP_011534498.1:p.Thr506=
XM_011536198.3:c.1328C=	XP_011534500.1:p.Thr443=
XM_024446573.1:c.1538C=	XP_024302341.1:p.Thr513=
XR_001743697.2:n.1569C=
XR_942606.2:n.1620C=
NM_032861.4:c.1538C= MANE Select	NP_116250.3:p.Thr513=
NR_073096.2:n.1453C=