Canonical Allele Identifier: CA2680956418

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114686-A-AGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114686_158114687insGTT , CM000668.2:g.158114686_158114687insGTT	GRCh38
NC_000006.11:g.158535718_158535719insGTT , CM000668.1:g.158535718_158535719insGTT	GRCh37
NC_000006.10:g.158455706_158455707insGTT	NCBI36
NG_032889.1:g.58594_58595insAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+102_*1404+103insAAC	ENSP00000475855.1:n.*1404+102_*1404+103insAAC
ENST00000642244.1:c.1594+102_1594+103insAAC	ENSP00000493554.1:n.1594+102_1594+103insAAC
ENST00000642903.1:c.*22_*23insAAC	ENSP00000493559.1:n.*22_*23insAAC
ENST00000644972.1:c.1684+102_1684+103insAAC	ENSP00000496451.1:n.1684+102_1684+103insAAC
ENST00000645077.1:c.*1305+102_*1305+103insAAC	ENSP00000496113.1:n.*1305+102_*1305+103insAAC
ENST00000645172.1:c.*1386+102_*1386+103insAAC	ENSP00000495367.1:n.*1386+102_*1386+103insAAC
ENST00000646190.1:n.3015+102_3015+103insAAC
ENST00000646208.1:c.1420+102_1420+103insAAC	ENSP00000493723.1:n.1420+102_1420+103insAAC
ENST00000646410.1:c.1555+102_1555+103insAAC	ENSP00000494205.1:n.1555+102_1555+103insAAC
ENST00000646562.1:c.*1620_*1621insAAC	ENSP00000496087.1:n.*1620_*1621insAAC
ENST00000647468.2:c.1684+102_1684+103insAAC MANE Select	ENSP00000496731.1:n.1684+102_1684+103insAAC
ENST00000648111.1:c.*1372+102_*1372+103insAAC	ENSP00000497275.1:n.*1372+102_*1372+103insAAC
ENST00000367104.7:c.1684+102_1684+103insAAC	ENSP00000356071.3:n.1684+102_1684+103insAAC
ENST00000606965.5:c.*347_*348insAAC	ENSP00000475808.1:n.*347_*348insAAC
ENST00000607071.5:c.*1618+102_*1618+103insAAC	ENSP00000475855.1:n.*1618+102_*1618+103insAAC
ENST00000607742.5:c.*2962+102_*2962+103insAAC	ENSP00000475523.1:n.*2962+102_*2962+103insAAC
NM_032861.3:c.1684+102_1684+103insAAC	NP_116250.3:n.1684+102_1684+103insAAC
NR_073096.1:n.1719_1720insAAC
XM_006715586.1:c.1474+102_1474+103insAAC	XP_006715649.1:n.1474+102_1474+103insAAC
XM_011536196.1:c.1663+102_1663+103insAAC	XP_011534498.1:n.1663+102_1663+103insAAC
XM_011536197.1:c.1570+102_1570+103insAAC	XP_011534499.1:n.1570+102_1570+103insAAC
XM_011536198.1:c.1474+102_1474+103insAAC	XP_011534500.1:n.1474+102_1474+103insAAC
XM_006715586.3:c.1474+102_1474+103insAAC	XP_006715649.1:n.1474+102_1474+103insAAC
XM_011536196.3:c.1663+102_1663+103insAAC	XP_011534498.1:n.1663+102_1663+103insAAC
XM_011536198.3:c.1474+102_1474+103insAAC	XP_011534500.1:n.1474+102_1474+103insAAC
XM_024446573.1:c.1684+102_1684+103insAAC	XP_024302341.1:n.1684+102_1684+103insAAC
XR_001743697.2:n.1715+102_1715+103insAAC
XR_942606.2:n.1766+102_1766+103insAAC
NM_032861.4:c.1684+102_1684+103insAAC MANE Select	NP_116250.3:n.1684+102_1684+103insAAC
NR_073096.2:n.1701_1702insAAC