Canonical Allele Identifier: CA1096370588

Gene: SERAC1

Linked Data

• dbSNP Id: rs1784259082

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158115310_158115311del , CM000668.2:g.158115310_158115311del	GRCh38
NC_000006.11:g.158536342_158536343del , CM000668.1:g.158536342_158536343del	GRCh37
NC_000006.10:g.158456330_158456331del	NCBI36
NG_032889.1:g.57974_57975del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.714-336_714-335del	ENSP00000391168.2:n.714-336_714-335del
ENST00000607071.6:c.*1222-336_*1222-335del	ENSP00000475855.1:n.*1222-336_*1222-335del
ENST00000642244.1:c.1412-336_1412-335del	ENSP00000493554.1:n.1412-336_1412-335del
ENST00000642903.1:c.1502-336_1502-335del	ENSP00000493559.1:n.1502-336_1502-335del
ENST00000644972.1:c.1502-336_1502-335del	ENSP00000496451.1:n.1502-336_1502-335del
ENST00000645077.1:c.*1123-336_*1123-335del	ENSP00000496113.1:n.*1123-336_*1123-335del
ENST00000645172.1:c.*1204-336_*1204-335del	ENSP00000495367.1:n.*1204-336_*1204-335del
ENST00000646190.1:n.2833-336_2833-335del
ENST00000646208.1:c.1238-336_1238-335del	ENSP00000493723.1:n.1238-336_1238-335del
ENST00000646410.1:c.1373-336_1373-335del	ENSP00000494205.1:n.1373-336_1373-335del
ENST00000646562.1:c.*1336-336_*1336-335del	ENSP00000496087.1:n.*1336-336_*1336-335del
ENST00000647468.2:c.1502-336_1502-335del MANE Select	ENSP00000496731.1:n.1502-336_1502-335del
ENST00000648111.1:c.*1190-336_*1190-335del	ENSP00000497275.1:n.*1190-336_*1190-335del
ENST00000367101.5:c.1546-336_1546-335del	ENSP00000356068.1:n.1546-336_1546-335del
ENST00000367104.7:c.1502-336_1502-335del	ENSP00000356071.3:n.1502-336_1502-335del
ENST00000435180.5:c.227-336_227-335del	ENSP00000391168.1:n.227-336_227-335del
ENST00000606965.5:c.*63-336_*63-335del	ENSP00000475808.1:n.*63-336_*63-335del
ENST00000607071.5:c.*1436-336_*1436-335del	ENSP00000475855.1:n.*1436-336_*1436-335del
ENST00000607742.5:c.*2780-336_*2780-335del	ENSP00000475523.1:n.*2780-336_*2780-335del
NM_032861.3:c.1502-336_1502-335del	NP_116250.3:n.1502-336_1502-335del
NR_073096.1:n.1435-336_1435-335del
XM_006715586.1:c.1292-336_1292-335del	XP_006715649.1:n.1292-336_1292-335del
XM_011536196.1:c.1481-336_1481-335del	XP_011534498.1:n.1481-336_1481-335del
XM_011536197.1:c.1388-336_1388-335del	XP_011534499.1:n.1388-336_1388-335del
XM_011536198.1:c.1292-336_1292-335del	XP_011534500.1:n.1292-336_1292-335del
XM_006715586.3:c.1292-336_1292-335del	XP_006715649.1:n.1292-336_1292-335del
XM_011536196.3:c.1481-336_1481-335del	XP_011534498.1:n.1481-336_1481-335del
XM_011536198.3:c.1292-336_1292-335del	XP_011534500.1:n.1292-336_1292-335del
XM_024446573.1:c.1502-336_1502-335del	XP_024302341.1:n.1502-336_1502-335del
XR_001743697.2:n.1533-336_1533-335del
XR_942606.2:n.1584-336_1584-335del
NM_032861.4:c.1502-336_1502-335del MANE Select	NP_116250.3:n.1502-336_1502-335del
NR_073096.2:n.1417-336_1417-335del