Canonical Allele Identifier: CA1675959466

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114907G= , CM000668.2:g.158114907G=	GRCh38
NC_000006.11:g.158535939G= , CM000668.1:g.158535939G=	GRCh37
NC_000006.10:g.158455927G=	NCBI36
NG_032889.1:g.58374C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.778C=	ENSP00000391168.2:n.778C=
ENST00000607071.6:c.*1286C=	ENSP00000475855.1:n.*1286C=
ENST00000642244.1:c.1476C=	ENSP00000493554.1:p.Asn492=
ENST00000642903.1:c.1566C=	ENSP00000493559.1:p.Asn522=
ENST00000644972.1:c.1566C=	ENSP00000496451.1:p.Asn522=
ENST00000645077.1:c.*1187C=	ENSP00000496113.1:n.*1187C=
ENST00000645172.1:c.*1268C=	ENSP00000495367.1:n.*1268C=
ENST00000646190.1:n.2897C=
ENST00000646208.1:c.1302C=	ENSP00000493723.1:p.Asn434=
ENST00000646410.1:c.1437C=	ENSP00000494205.1:p.Asn479=
ENST00000646562.1:c.*1400C=	ENSP00000496087.1:n.*1400C=
ENST00000647468.2:c.1566C= MANE Select	ENSP00000496731.1:p.Asn522=
ENST00000648111.1:c.*1254C=	ENSP00000497275.1:n.*1254C=
ENST00000367101.5:c.*14C=	ENSP00000356068.1:n.*14C=
ENST00000367104.7:c.1566C=	ENSP00000356071.3:p.Asn522=
ENST00000435180.5:c.291C=	ENSP00000391168.1:p.Asn97=
ENST00000606965.5:c.*127C=	ENSP00000475808.1:n.*127C=
ENST00000607071.5:c.*1500C=	ENSP00000475855.1:n.*1500C=
ENST00000607742.5:c.*2844C=	ENSP00000475523.1:n.*2844C=
NM_032861.3:c.1566C=	NP_116250.3:p.Asn522=
NR_073096.1:n.1499C=
XM_006715586.1:c.1356C=	XP_006715649.1:p.Asn452=
XM_011536196.1:c.1545C=	XP_011534498.1:p.Asn515=
XM_011536197.1:c.1452C=	XP_011534499.1:p.Asn484=
XM_011536198.1:c.1356C=	XP_011534500.1:p.Asn452=
XM_006715586.3:c.1356C=	XP_006715649.1:p.Asn452=
XM_011536196.3:c.1545C=	XP_011534498.1:p.Asn515=
XM_011536198.3:c.1356C=	XP_011534500.1:p.Asn452=
XM_024446573.1:c.1566C=	XP_024302341.1:p.Asn522=
XR_001743697.2:n.1597C=
XR_942606.2:n.1648C=
NM_032861.4:c.1566C= MANE Select	NP_116250.3:p.Asn522=
NR_073096.2:n.1481C=