Canonical Allele Identifier: CA2680956706

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114778-A-AAAAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114780_158114784dup , CM000668.2:g.158114780_158114784dup	GRCh38
NC_000006.11:g.158535812_158535816dup , CM000668.1:g.158535812_158535816dup	GRCh37
NC_000006.10:g.158455800_158455804dup	NCBI36
NG_032889.1:g.58498_58502dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+6_*1404+10dup	ENSP00000475855.1:n.*1404+6_*1404+10dup
ENST00000642244.1:c.1594+6_1594+10dup	ENSP00000493554.1:n.1594+6_1594+10dup
ENST00000642903.1:c.1690_1694dup	ENSP00000493559.1:p.Phe565LeufsTer?
ENST00000644972.1:c.1684+6_1684+10dup	ENSP00000496451.1:n.1684+6_1684+10dup
ENST00000645077.1:c.*1305+6_*1305+10dup	ENSP00000496113.1:n.*1305+6_*1305+10dup
ENST00000645172.1:c.*1386+6_*1386+10dup	ENSP00000495367.1:n.*1386+6_*1386+10dup
ENST00000646190.1:n.3015+6_3015+10dup
ENST00000646208.1:c.1420+6_1420+10dup	ENSP00000493723.1:n.1420+6_1420+10dup
ENST00000646410.1:c.1555+6_1555+10dup	ENSP00000494205.1:n.1555+6_1555+10dup
ENST00000646562.1:c.*1524_*1528dup	ENSP00000496087.1:n.*1524_*1528dup
ENST00000647468.2:c.1684+6_1684+10dup MANE Select	ENSP00000496731.1:n.1684+6_1684+10dup
ENST00000648111.1:c.*1372+6_*1372+10dup	ENSP00000497275.1:n.*1372+6_*1372+10dup
ENST00000367101.5:c.*138_*142dup	ENSP00000356068.1:n.*138_*142dup
ENST00000367104.7:c.1684+6_1684+10dup	ENSP00000356071.3:n.1684+6_1684+10dup
ENST00000435180.5:c.415_419dup	ENSP00000391168.1:p.Phe140LeufsTer?
ENST00000606965.5:c.*251_*255dup	ENSP00000475808.1:n.*251_*255dup
ENST00000607071.5:c.*1618+6_*1618+10dup	ENSP00000475855.1:n.*1618+6_*1618+10dup
ENST00000607742.5:c.*2962+6_*2962+10dup	ENSP00000475523.1:n.*2962+6_*2962+10dup
NM_032861.3:c.1684+6_1684+10dup	NP_116250.3:n.1684+6_1684+10dup
NR_073096.1:n.1623_1627dup
XM_006715586.1:c.1474+6_1474+10dup	XP_006715649.1:n.1474+6_1474+10dup
XM_011536196.1:c.1663+6_1663+10dup	XP_011534498.1:n.1663+6_1663+10dup
XM_011536197.1:c.1570+6_1570+10dup	XP_011534499.1:n.1570+6_1570+10dup
XM_011536198.1:c.1474+6_1474+10dup	XP_011534500.1:n.1474+6_1474+10dup
XM_006715586.3:c.1474+6_1474+10dup	XP_006715649.1:n.1474+6_1474+10dup
XM_011536196.3:c.1663+6_1663+10dup	XP_011534498.1:n.1663+6_1663+10dup
XM_011536198.3:c.1474+6_1474+10dup	XP_011534500.1:n.1474+6_1474+10dup
XM_024446573.1:c.1684+6_1684+10dup	XP_024302341.1:n.1684+6_1684+10dup
XR_001743697.2:n.1715+6_1715+10dup
XR_942606.2:n.1766+6_1766+10dup
NM_032861.4:c.1684+6_1684+10dup MANE Select	NP_116250.3:n.1684+6_1684+10dup
NR_073096.2:n.1605_1609dup