Canonical Allele Identifier: CA1675959439

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114870G= , CM000668.2:g.158114870G=	GRCh38
NC_000006.11:g.158535902G= , CM000668.1:g.158535902G=	GRCh37
NC_000006.10:g.158455890G=	NCBI36
NG_032889.1:g.58411C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.815C=	ENSP00000391168.2:n.815C=
ENST00000607071.6:c.*1323C=	ENSP00000475855.1:n.*1323C=
ENST00000642244.1:c.1513C=	ENSP00000493554.1:p.His505=
ENST00000642903.1:c.1603C=	ENSP00000493559.1:p.His535=
ENST00000644972.1:c.1603C=	ENSP00000496451.1:p.His535=
ENST00000645077.1:c.*1224C=	ENSP00000496113.1:n.*1224C=
ENST00000645172.1:c.*1305C=	ENSP00000495367.1:n.*1305C=
ENST00000646190.1:n.2934C=
ENST00000646208.1:c.1339C=	ENSP00000493723.1:p.His447=
ENST00000646410.1:c.1474C=	ENSP00000494205.1:p.His492=
ENST00000646562.1:c.*1437C=	ENSP00000496087.1:n.*1437C=
ENST00000647468.2:c.1603C= MANE Select	ENSP00000496731.1:p.His535=
ENST00000648111.1:c.*1291C=	ENSP00000497275.1:n.*1291C=
ENST00000367101.5:c.*51C=	ENSP00000356068.1:n.*51C=
ENST00000367104.7:c.1603C=	ENSP00000356071.3:p.His535=
ENST00000435180.5:c.328C=	ENSP00000391168.1:p.His110=
ENST00000606965.5:c.*164C=	ENSP00000475808.1:n.*164C=
ENST00000607071.5:c.*1537C=	ENSP00000475855.1:n.*1537C=
ENST00000607742.5:c.*2881C=	ENSP00000475523.1:n.*2881C=
NM_032861.3:c.1603C=	NP_116250.3:p.His535=
NR_073096.1:n.1536C=
XM_006715586.1:c.1393C=	XP_006715649.1:p.His465=
XM_011536196.1:c.1582C=	XP_011534498.1:p.His528=
XM_011536197.1:c.1489C=	XP_011534499.1:p.His497=
XM_011536198.1:c.1393C=	XP_011534500.1:p.His465=
XM_006715586.3:c.1393C=	XP_006715649.1:p.His465=
XM_011536196.3:c.1582C=	XP_011534498.1:p.His528=
XM_011536198.3:c.1393C=	XP_011534500.1:p.His465=
XM_024446573.1:c.1603C=	XP_024302341.1:p.His535=
XR_001743697.2:n.1634C=
XR_942606.2:n.1685C=
NM_032861.4:c.1603C= MANE Select	NP_116250.3:p.His535=
NR_073096.2:n.1518C=