Canonical Allele Identifier: CA2680956770

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114935-G-GTACA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114937_158114938insCATA , CM000668.2:g.158114937_158114938insCATA	GRCh38
NC_000006.11:g.158535969_158535970insCATA , CM000668.1:g.158535969_158535970insCATA	GRCh37
NC_000006.10:g.158455957_158455958insCATA	NCBI36
NG_032889.1:g.58345_58346insTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.749_750insTGTA	ENSP00000391168.2:n.749_750insTGTA
ENST00000607071.6:c.*1257_*1258insTGTA	ENSP00000475855.1:n.*1257_*1258insTGTA
ENST00000642244.1:c.1447_1448insTGTA	ENSP00000493554.1:p.Thr483MetfsTer20
ENST00000642903.1:c.1537_1538insTGTA	ENSP00000493559.1:p.Thr513MetfsTer20
ENST00000644972.1:c.1537_1538insTGTA	ENSP00000496451.1:p.Thr513MetfsTer20
ENST00000645077.1:c.*1158_*1159insTGTA	ENSP00000496113.1:n.*1158_*1159insTGTA
ENST00000645172.1:c.*1239_*1240insTGTA	ENSP00000495367.1:n.*1239_*1240insTGTA
ENST00000646190.1:n.2868_2869insTGTA
ENST00000646208.1:c.1273_1274insTGTA	ENSP00000493723.1:p.Thr425MetfsTer20
ENST00000646410.1:c.1408_1409insTGTA	ENSP00000494205.1:p.Thr470MetfsTer20
ENST00000646562.1:c.*1371_*1372insTGTA	ENSP00000496087.1:n.*1371_*1372insTGTA
ENST00000647468.2:c.1537_1538insTGTA MANE Select	ENSP00000496731.1:p.Thr513MetfsTer20
ENST00000648111.1:c.*1225_*1226insTGTA	ENSP00000497275.1:n.*1225_*1226insTGTA
ENST00000367101.5:c.1581_1582insTGTA	ENSP00000356068.1:p.Arg528CysfsTer?
ENST00000367104.7:c.1537_1538insTGTA	ENSP00000356071.3:p.Thr513MetfsTer20
ENST00000435180.5:c.262_263insTGTA	ENSP00000391168.1:p.Thr88MetfsTer20
ENST00000606965.5:c.*98_*99insTGTA	ENSP00000475808.1:n.*98_*99insTGTA
ENST00000607071.5:c.*1471_*1472insTGTA	ENSP00000475855.1:n.*1471_*1472insTGTA
ENST00000607742.5:c.*2815_*2816insTGTA	ENSP00000475523.1:n.*2815_*2816insTGTA
NM_032861.3:c.1537_1538insTGTA	NP_116250.3:p.Thr513MetfsTer20
NR_073096.1:n.1470_1471insTGTA
XM_006715586.1:c.1327_1328insTGTA	XP_006715649.1:p.Thr443MetfsTer20
XM_011536196.1:c.1516_1517insTGTA	XP_011534498.1:p.Thr506MetfsTer20
XM_011536197.1:c.1423_1424insTGTA	XP_011534499.1:p.Thr475MetfsTer20
XM_011536198.1:c.1327_1328insTGTA	XP_011534500.1:p.Thr443MetfsTer20
XM_006715586.3:c.1327_1328insTGTA	XP_006715649.1:p.Thr443MetfsTer20
XM_011536196.3:c.1516_1517insTGTA	XP_011534498.1:p.Thr506MetfsTer20
XM_011536198.3:c.1327_1328insTGTA	XP_011534500.1:p.Thr443MetfsTer20
XM_024446573.1:c.1537_1538insTGTA	XP_024302341.1:p.Thr513MetfsTer20
XR_001743697.2:n.1568_1569insTGTA
XR_942606.2:n.1619_1620insTGTA
NM_032861.4:c.1537_1538insTGTA MANE Select	NP_116250.3:p.Thr513MetfsTer20
NR_073096.2:n.1452_1453insTGTA