Canonical Allele Identifier: CA1675959555

Gene: SERAC1

Linked Data

• dbSNP Id: rs1784251692

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158115039_158115042del , CM000668.2:g.158115039_158115042del	GRCh38
NC_000006.11:g.158536071_158536074del , CM000668.1:g.158536071_158536074del	GRCh37
NC_000006.10:g.158456059_158456062del	NCBI36
NG_032889.1:g.58242_58245del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.714-68_714-65del	ENSP00000391168.2:n.714-68_714-65del
ENST00000607071.6:c.*1222-68_*1222-65del	ENSP00000475855.1:n.*1222-68_*1222-65del
ENST00000642244.1:c.1412-68_1412-65del	ENSP00000493554.1:n.1412-68_1412-65del
ENST00000642903.1:c.1502-68_1502-65del	ENSP00000493559.1:n.1502-68_1502-65del
ENST00000644972.1:c.1502-68_1502-65del	ENSP00000496451.1:n.1502-68_1502-65del
ENST00000645077.1:c.*1123-68_*1123-65del	ENSP00000496113.1:n.*1123-68_*1123-65del
ENST00000645172.1:c.*1204-68_*1204-65del	ENSP00000495367.1:n.*1204-68_*1204-65del
ENST00000646190.1:n.2833-68_2833-65del
ENST00000646208.1:c.1238-68_1238-65del	ENSP00000493723.1:n.1238-68_1238-65del
ENST00000646410.1:c.1373-68_1373-65del	ENSP00000494205.1:n.1373-68_1373-65del
ENST00000646562.1:c.*1336-68_*1336-65del	ENSP00000496087.1:n.*1336-68_*1336-65del
ENST00000647468.2:c.1502-68_1502-65del MANE Select	ENSP00000496731.1:n.1502-68_1502-65del
ENST00000648111.1:c.*1190-68_*1190-65del	ENSP00000497275.1:n.*1190-68_*1190-65del
ENST00000367101.5:c.1546-68_1546-65del	ENSP00000356068.1:n.1546-68_1546-65del
ENST00000367104.7:c.1502-68_1502-65del	ENSP00000356071.3:n.1502-68_1502-65del
ENST00000435180.5:c.227-68_227-65del	ENSP00000391168.1:n.227-68_227-65del
ENST00000606965.5:c.*63-68_*63-65del	ENSP00000475808.1:n.*63-68_*63-65del
ENST00000607071.5:c.*1436-68_*1436-65del	ENSP00000475855.1:n.*1436-68_*1436-65del
ENST00000607742.5:c.*2780-68_*2780-65del	ENSP00000475523.1:n.*2780-68_*2780-65del
NM_032861.3:c.1502-68_1502-65del	NP_116250.3:n.1502-68_1502-65del
NR_073096.1:n.1435-68_1435-65del
XM_006715586.1:c.1292-68_1292-65del	XP_006715649.1:n.1292-68_1292-65del
XM_011536196.1:c.1481-68_1481-65del	XP_011534498.1:n.1481-68_1481-65del
XM_011536197.1:c.1388-68_1388-65del	XP_011534499.1:n.1388-68_1388-65del
XM_011536198.1:c.1292-68_1292-65del	XP_011534500.1:n.1292-68_1292-65del
XM_006715586.3:c.1292-68_1292-65del	XP_006715649.1:n.1292-68_1292-65del
XM_011536196.3:c.1481-68_1481-65del	XP_011534498.1:n.1481-68_1481-65del
XM_011536198.3:c.1292-68_1292-65del	XP_011534500.1:n.1292-68_1292-65del
XM_024446573.1:c.1502-68_1502-65del	XP_024302341.1:n.1502-68_1502-65del
XR_001743697.2:n.1533-68_1533-65del
XR_942606.2:n.1584-68_1584-65del
NM_032861.4:c.1502-68_1502-65del MANE Select	NP_116250.3:n.1502-68_1502-65del
NR_073096.2:n.1417-68_1417-65del