Canonical Allele Identifier: CA2680956648

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114719-A-AGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114719_158114720insGAG , CM000668.2:g.158114719_158114720insGAG	GRCh38
NC_000006.11:g.158535751_158535752insGAG , CM000668.1:g.158535751_158535752insGAG	GRCh37
NC_000006.10:g.158455739_158455740insGAG	NCBI36
NG_032889.1:g.58561_58562insCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+69_*1404+70insCTC	ENSP00000475855.1:n.*1404+69_*1404+70insCTC
ENST00000642244.1:c.1594+69_1594+70insCTC	ENSP00000493554.1:n.1594+69_1594+70insCTC
ENST00000642903.1:c.1753_1754insCTC	ENSP00000493559.1:p.Phe585delinsSerLeu
ENST00000644972.1:c.1684+69_1684+70insCTC	ENSP00000496451.1:n.1684+69_1684+70insCTC
ENST00000645077.1:c.*1305+69_*1305+70insCTC	ENSP00000496113.1:n.*1305+69_*1305+70insCTC
ENST00000645172.1:c.*1386+69_*1386+70insCTC	ENSP00000495367.1:n.*1386+69_*1386+70insCTC
ENST00000646190.1:n.3015+69_3015+70insCTC
ENST00000646208.1:c.1420+69_1420+70insCTC	ENSP00000493723.1:n.1420+69_1420+70insCTC
ENST00000646410.1:c.1555+69_1555+70insCTC	ENSP00000494205.1:n.1555+69_1555+70insCTC
ENST00000646562.1:c.*1587_*1588insCTC	ENSP00000496087.1:n.*1587_*1588insCTC
ENST00000647468.2:c.1684+69_1684+70insCTC MANE Select	ENSP00000496731.1:n.1684+69_1684+70insCTC
ENST00000648111.1:c.*1372+69_*1372+70insCTC	ENSP00000497275.1:n.*1372+69_*1372+70insCTC
ENST00000367104.7:c.1684+69_1684+70insCTC	ENSP00000356071.3:n.1684+69_1684+70insCTC
ENST00000435180.5:c.478_479insCTC	ENSP00000391168.1:p.Phe160delinsSerLeu
ENST00000606965.5:c.*314_*315insCTC	ENSP00000475808.1:n.*314_*315insCTC
ENST00000607071.5:c.*1618+69_*1618+70insCTC	ENSP00000475855.1:n.*1618+69_*1618+70insCTC
ENST00000607742.5:c.*2962+69_*2962+70insCTC	ENSP00000475523.1:n.*2962+69_*2962+70insCTC
NM_032861.3:c.1684+69_1684+70insCTC	NP_116250.3:n.1684+69_1684+70insCTC
NR_073096.1:n.1686_1687insCTC
XM_006715586.1:c.1474+69_1474+70insCTC	XP_006715649.1:n.1474+69_1474+70insCTC
XM_011536196.1:c.1663+69_1663+70insCTC	XP_011534498.1:n.1663+69_1663+70insCTC
XM_011536197.1:c.1570+69_1570+70insCTC	XP_011534499.1:n.1570+69_1570+70insCTC
XM_011536198.1:c.1474+69_1474+70insCTC	XP_011534500.1:n.1474+69_1474+70insCTC
XM_006715586.3:c.1474+69_1474+70insCTC	XP_006715649.1:n.1474+69_1474+70insCTC
XM_011536196.3:c.1663+69_1663+70insCTC	XP_011534498.1:n.1663+69_1663+70insCTC
XM_011536198.3:c.1474+69_1474+70insCTC	XP_011534500.1:n.1474+69_1474+70insCTC
XM_024446573.1:c.1684+69_1684+70insCTC	XP_024302341.1:n.1684+69_1684+70insCTC
XR_001743697.2:n.1715+69_1715+70insCTC
XR_942606.2:n.1766+69_1766+70insCTC
NM_032861.4:c.1684+69_1684+70insCTC MANE Select	NP_116250.3:n.1684+69_1684+70insCTC
NR_073096.2:n.1668_1669insCTC