Canonical Allele Identifier: CA1675959452

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114883_158114884delinsAT , CM000668.2:g.158114883_158114884delinsAT	GRCh38
NC_000006.11:g.158535915_158535916delinsAT , CM000668.1:g.158535915_158535916delinsAT	GRCh37
NC_000006.10:g.158455903_158455904delinsAT	NCBI36
NG_032889.1:g.58397_58398delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.801_802delinsAT	ENSP00000391168.2:n.801_802delinsAT
ENST00000607071.6:c.*1309_*1310delinsAT	ENSP00000475855.1:n.*1309_*1310delinsAT
ENST00000642244.1:c.1499_1500delinsAT	ENSP00000493554.1:p.Tyr500=
ENST00000642903.1:c.1589_1590delinsAT	ENSP00000493559.1:p.Tyr530=
ENST00000644972.1:c.1589_1590delinsAT	ENSP00000496451.1:p.Tyr530=
ENST00000645077.1:c.*1210_*1211delinsAT	ENSP00000496113.1:n.*1210_*1211delinsAT
ENST00000645172.1:c.*1291_*1292delinsAT	ENSP00000495367.1:n.*1291_*1292delinsAT
ENST00000646190.1:n.2920_2921delinsAT
ENST00000646208.1:c.1325_1326delinsAT	ENSP00000493723.1:p.Tyr442=
ENST00000646410.1:c.1460_1461delinsAT	ENSP00000494205.1:p.Tyr487=
ENST00000646562.1:c.*1423_*1424delinsAT	ENSP00000496087.1:n.*1423_*1424delinsAT
ENST00000647468.2:c.1589_1590delinsAT MANE Select	ENSP00000496731.1:p.Tyr530=
ENST00000648111.1:c.*1277_*1278delinsAT	ENSP00000497275.1:n.*1277_*1278delinsAT
ENST00000367101.5:c.*37_*38delinsAT	ENSP00000356068.1:n.*37_*38delinsAT
ENST00000367104.7:c.1589_1590delinsAT	ENSP00000356071.3:p.Tyr530=
ENST00000435180.5:c.314_315delinsAT	ENSP00000391168.1:p.Tyr105=
ENST00000606965.5:c.*150_*151delinsAT	ENSP00000475808.1:n.*150_*151delinsAT
ENST00000607071.5:c.*1523_*1524delinsAT	ENSP00000475855.1:n.*1523_*1524delinsAT
ENST00000607742.5:c.*2867_*2868delinsAT	ENSP00000475523.1:n.*2867_*2868delinsAT
NM_032861.3:c.1589_1590delinsAT	NP_116250.3:p.Tyr530=
NR_073096.1:n.1522_1523delinsAT
XM_006715586.1:c.1379_1380delinsAT	XP_006715649.1:p.Tyr460=
XM_011536196.1:c.1568_1569delinsAT	XP_011534498.1:p.Tyr523=
XM_011536197.1:c.1475_1476delinsAT	XP_011534499.1:p.Tyr492=
XM_011536198.1:c.1379_1380delinsAT	XP_011534500.1:p.Tyr460=
XM_006715586.3:c.1379_1380delinsAT	XP_006715649.1:p.Tyr460=
XM_011536196.3:c.1568_1569delinsAT	XP_011534498.1:p.Tyr523=
XM_011536198.3:c.1379_1380delinsAT	XP_011534500.1:p.Tyr460=
XM_024446573.1:c.1589_1590delinsAT	XP_024302341.1:p.Tyr530=
XR_001743697.2:n.1620_1621delinsAT
XR_942606.2:n.1671_1672delinsAT
NM_032861.4:c.1589_1590delinsAT MANE Select	NP_116250.3:p.Tyr530=
NR_073096.2:n.1504_1505delinsAT