Canonical Allele Identifier: CA2713757890

Gene: SERAC1

Linked Data

• dbSNP Id: rs2128410651

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114908_158114910del , CM000668.2:g.158114908_158114910del	GRCh38
NC_000006.11:g.158535940_158535942del , CM000668.1:g.158535940_158535942del	GRCh37
NC_000006.10:g.158455928_158455930del	NCBI36
NG_032889.1:g.58374_58376del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.778_780del	ENSP00000391168.2:n.778_780del
ENST00000607071.6:c.*1286_*1288del	ENSP00000475855.1:n.*1286_*1288del
ENST00000642244.1:c.1476_1478del	ENSP00000493554.1:p.Asn493del
ENST00000642903.1:c.1566_1568del	ENSP00000493559.1:p.Asn523del
ENST00000644972.1:c.1566_1568del	ENSP00000496451.1:p.Asn523del
ENST00000645077.1:c.*1187_*1189del	ENSP00000496113.1:n.*1187_*1189del
ENST00000645172.1:c.*1268_*1270del	ENSP00000495367.1:n.*1268_*1270del
ENST00000646190.1:n.2897_2899del
ENST00000646208.1:c.1302_1304del	ENSP00000493723.1:p.Asn435del
ENST00000646410.1:c.1437_1439del	ENSP00000494205.1:p.Asn480del
ENST00000646562.1:c.*1400_*1402del	ENSP00000496087.1:n.*1400_*1402del
ENST00000647468.2:c.1566_1568del MANE Select	ENSP00000496731.1:p.Asn523del
ENST00000648111.1:c.*1254_*1256del	ENSP00000497275.1:n.*1254_*1256del
ENST00000367101.5:c.*14_*16del	ENSP00000356068.1:n.*14_*16del
ENST00000367104.7:c.1566_1568del	ENSP00000356071.3:p.Asn523del
ENST00000435180.5:c.291_293del	ENSP00000391168.1:p.Asn98del
ENST00000606965.5:c.*127_*129del	ENSP00000475808.1:n.*127_*129del
ENST00000607071.5:c.*1500_*1502del	ENSP00000475855.1:n.*1500_*1502del
ENST00000607742.5:c.*2844_*2846del	ENSP00000475523.1:n.*2844_*2846del
NM_032861.3:c.1566_1568del	NP_116250.3:p.Asn523del
NR_073096.1:n.1499_1501del
XM_006715586.1:c.1356_1358del	XP_006715649.1:p.Asn453del
XM_011536196.1:c.1545_1547del	XP_011534498.1:p.Asn516del
XM_011536197.1:c.1452_1454del	XP_011534499.1:p.Asn485del
XM_011536198.1:c.1356_1358del	XP_011534500.1:p.Asn453del
XM_006715586.3:c.1356_1358del	XP_006715649.1:p.Asn453del
XM_011536196.3:c.1545_1547del	XP_011534498.1:p.Asn516del
XM_011536198.3:c.1356_1358del	XP_011534500.1:p.Asn453del
XM_024446573.1:c.1566_1568del	XP_024302341.1:p.Asn523del
XR_001743697.2:n.1597_1599del
XR_942606.2:n.1648_1650del
NM_032861.4:c.1566_1568del MANE Select	NP_116250.3:p.Asn523del
NR_073096.2:n.1481_1483del