Canonical Allele Identifier: CA1675959580

Gene: SERAC1

Linked Data

• dbSNP Id: rs1784252887
• gnomAD v4: 6-158115073-GCTTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158115078_158115081del , CM000668.2:g.158115078_158115081del	GRCh38
NC_000006.11:g.158536110_158536113del , CM000668.1:g.158536110_158536113del	GRCh37
NC_000006.10:g.158456098_158456101del	NCBI36
NG_032889.1:g.58204_58207del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.714-106_714-103del	ENSP00000391168.2:n.714-106_714-103del
ENST00000607071.6:c.*1222-106_*1222-103del	ENSP00000475855.1:n.*1222-106_*1222-103del
ENST00000642244.1:c.1412-106_1412-103del	ENSP00000493554.1:n.1412-106_1412-103del
ENST00000642903.1:c.1502-106_1502-103del	ENSP00000493559.1:n.1502-106_1502-103del
ENST00000644972.1:c.1502-106_1502-103del	ENSP00000496451.1:n.1502-106_1502-103del
ENST00000645077.1:c.*1123-106_*1123-103del	ENSP00000496113.1:n.*1123-106_*1123-103del
ENST00000645172.1:c.*1204-106_*1204-103del	ENSP00000495367.1:n.*1204-106_*1204-103del
ENST00000646190.1:n.2833-106_2833-103del
ENST00000646208.1:c.1238-106_1238-103del	ENSP00000493723.1:n.1238-106_1238-103del
ENST00000646410.1:c.1373-106_1373-103del	ENSP00000494205.1:n.1373-106_1373-103del
ENST00000646562.1:c.*1336-106_*1336-103del	ENSP00000496087.1:n.*1336-106_*1336-103del
ENST00000647468.2:c.1502-106_1502-103del MANE Select	ENSP00000496731.1:n.1502-106_1502-103del
ENST00000648111.1:c.*1190-106_*1190-103del	ENSP00000497275.1:n.*1190-106_*1190-103del
ENST00000367101.5:c.1546-106_1546-103del	ENSP00000356068.1:n.1546-106_1546-103del
ENST00000367104.7:c.1502-106_1502-103del	ENSP00000356071.3:n.1502-106_1502-103del
ENST00000435180.5:c.227-106_227-103del	ENSP00000391168.1:n.227-106_227-103del
ENST00000606965.5:c.*63-106_*63-103del	ENSP00000475808.1:n.*63-106_*63-103del
ENST00000607071.5:c.*1436-106_*1436-103del	ENSP00000475855.1:n.*1436-106_*1436-103del
ENST00000607742.5:c.*2780-106_*2780-103del	ENSP00000475523.1:n.*2780-106_*2780-103del
NM_032861.3:c.1502-106_1502-103del	NP_116250.3:n.1502-106_1502-103del
NR_073096.1:n.1435-106_1435-103del
XM_006715586.1:c.1292-106_1292-103del	XP_006715649.1:n.1292-106_1292-103del
XM_011536196.1:c.1481-106_1481-103del	XP_011534498.1:n.1481-106_1481-103del
XM_011536197.1:c.1388-106_1388-103del	XP_011534499.1:n.1388-106_1388-103del
XM_011536198.1:c.1292-106_1292-103del	XP_011534500.1:n.1292-106_1292-103del
XM_006715586.3:c.1292-106_1292-103del	XP_006715649.1:n.1292-106_1292-103del
XM_011536196.3:c.1481-106_1481-103del	XP_011534498.1:n.1481-106_1481-103del
XM_011536198.3:c.1292-106_1292-103del	XP_011534500.1:n.1292-106_1292-103del
XM_024446573.1:c.1502-106_1502-103del	XP_024302341.1:n.1502-106_1502-103del
XR_001743697.2:n.1533-106_1533-103del
XR_942606.2:n.1584-106_1584-103del
NM_032861.4:c.1502-106_1502-103del MANE Select	NP_116250.3:n.1502-106_1502-103del
NR_073096.2:n.1417-106_1417-103del