Canonical Allele Identifier: CA2773733438

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158115090_158115091dup , CM000668.2:g.158115090_158115091dup	GRCh38
NC_000006.11:g.158536122_158536123dup , CM000668.1:g.158536122_158536123dup	GRCh37
NC_000006.10:g.158456110_158456111dup	NCBI36
NG_032889.1:g.58196_58197dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.714-114_714-113dup	ENSP00000391168.2:n.714-114_714-113dup
ENST00000607071.6:c.*1222-114_*1222-113dup	ENSP00000475855.1:n.*1222-114_*1222-113dup
ENST00000642244.1:c.1412-114_1412-113dup	ENSP00000493554.1:n.1412-114_1412-113dup
ENST00000642903.1:c.1502-114_1502-113dup	ENSP00000493559.1:n.1502-114_1502-113dup
ENST00000644972.1:c.1502-114_1502-113dup	ENSP00000496451.1:n.1502-114_1502-113dup
ENST00000645077.1:c.*1123-114_*1123-113dup	ENSP00000496113.1:n.*1123-114_*1123-113dup
ENST00000645172.1:c.*1204-114_*1204-113dup	ENSP00000495367.1:n.*1204-114_*1204-113dup
ENST00000646190.1:n.2833-114_2833-113dup
ENST00000646208.1:c.1238-114_1238-113dup	ENSP00000493723.1:n.1238-114_1238-113dup
ENST00000646410.1:c.1373-114_1373-113dup	ENSP00000494205.1:n.1373-114_1373-113dup
ENST00000646562.1:c.*1336-114_*1336-113dup	ENSP00000496087.1:n.*1336-114_*1336-113dup
ENST00000647468.2:c.1502-114_1502-113dup MANE Select	ENSP00000496731.1:n.1502-114_1502-113dup
ENST00000648111.1:c.*1190-114_*1190-113dup	ENSP00000497275.1:n.*1190-114_*1190-113dup
ENST00000367101.5:c.1546-114_1546-113dup	ENSP00000356068.1:n.1546-114_1546-113dup
ENST00000367104.7:c.1502-114_1502-113dup	ENSP00000356071.3:n.1502-114_1502-113dup
ENST00000435180.5:c.227-114_227-113dup	ENSP00000391168.1:n.227-114_227-113dup
ENST00000606965.5:c.*63-114_*63-113dup	ENSP00000475808.1:n.*63-114_*63-113dup
ENST00000607071.5:c.*1436-114_*1436-113dup	ENSP00000475855.1:n.*1436-114_*1436-113dup
ENST00000607742.5:c.*2780-114_*2780-113dup	ENSP00000475523.1:n.*2780-114_*2780-113dup
NM_032861.3:c.1502-114_1502-113dup	NP_116250.3:n.1502-114_1502-113dup
NR_073096.1:n.1435-114_1435-113dup
XM_006715586.1:c.1292-114_1292-113dup	XP_006715649.1:n.1292-114_1292-113dup
XM_011536196.1:c.1481-114_1481-113dup	XP_011534498.1:n.1481-114_1481-113dup
XM_011536197.1:c.1388-114_1388-113dup	XP_011534499.1:n.1388-114_1388-113dup
XM_011536198.1:c.1292-114_1292-113dup	XP_011534500.1:n.1292-114_1292-113dup
XM_006715586.3:c.1292-114_1292-113dup	XP_006715649.1:n.1292-114_1292-113dup
XM_011536196.3:c.1481-114_1481-113dup	XP_011534498.1:n.1481-114_1481-113dup
XM_011536198.3:c.1292-114_1292-113dup	XP_011534500.1:n.1292-114_1292-113dup
XM_024446573.1:c.1502-114_1502-113dup	XP_024302341.1:n.1502-114_1502-113dup
XR_001743697.2:n.1533-114_1533-113dup
XR_942606.2:n.1584-114_1584-113dup
NM_032861.4:c.1502-114_1502-113dup MANE Select	NP_116250.3:n.1502-114_1502-113dup
NR_073096.2:n.1417-114_1417-113dup