Canonical Allele Identifier: CA2680956415

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114686-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114687_158114688del , CM000668.2:g.158114687_158114688del	GRCh38
NC_000006.11:g.158535719_158535720del , CM000668.1:g.158535719_158535720del	GRCh37
NC_000006.10:g.158455707_158455708del	NCBI36
NG_032889.1:g.58593_58594del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+101_*1404+102del	ENSP00000475855.1:n.*1404+101_*1404+102del
ENST00000642244.1:c.1594+101_1594+102del	ENSP00000493554.1:n.1594+101_1594+102del
ENST00000642903.1:c.*21_*22del	ENSP00000493559.1:n.*21_*22del
ENST00000644972.1:c.1684+101_1684+102del	ENSP00000496451.1:n.1684+101_1684+102del
ENST00000645077.1:c.*1305+101_*1305+102del	ENSP00000496113.1:n.*1305+101_*1305+102del
ENST00000645172.1:c.*1386+101_*1386+102del	ENSP00000495367.1:n.*1386+101_*1386+102del
ENST00000646190.1:n.3015+101_3015+102del
ENST00000646208.1:c.1420+101_1420+102del	ENSP00000493723.1:n.1420+101_1420+102del
ENST00000646410.1:c.1555+101_1555+102del	ENSP00000494205.1:n.1555+101_1555+102del
ENST00000646562.1:c.*1619_*1620del	ENSP00000496087.1:n.*1619_*1620del
ENST00000647468.2:c.1684+101_1684+102del MANE Select	ENSP00000496731.1:n.1684+101_1684+102del
ENST00000648111.1:c.*1372+101_*1372+102del	ENSP00000497275.1:n.*1372+101_*1372+102del
ENST00000367104.7:c.1684+101_1684+102del	ENSP00000356071.3:n.1684+101_1684+102del
ENST00000606965.5:c.*346_*347del	ENSP00000475808.1:n.*346_*347del
ENST00000607071.5:c.*1618+101_*1618+102del	ENSP00000475855.1:n.*1618+101_*1618+102del
ENST00000607742.5:c.*2962+101_*2962+102del	ENSP00000475523.1:n.*2962+101_*2962+102del
NM_032861.3:c.1684+101_1684+102del	NP_116250.3:n.1684+101_1684+102del
NR_073096.1:n.1718_1719del
XM_006715586.1:c.1474+101_1474+102del	XP_006715649.1:n.1474+101_1474+102del
XM_011536196.1:c.1663+101_1663+102del	XP_011534498.1:n.1663+101_1663+102del
XM_011536197.1:c.1570+101_1570+102del	XP_011534499.1:n.1570+101_1570+102del
XM_011536198.1:c.1474+101_1474+102del	XP_011534500.1:n.1474+101_1474+102del
XM_006715586.3:c.1474+101_1474+102del	XP_006715649.1:n.1474+101_1474+102del
XM_011536196.3:c.1663+101_1663+102del	XP_011534498.1:n.1663+101_1663+102del
XM_011536198.3:c.1474+101_1474+102del	XP_011534500.1:n.1474+101_1474+102del
XM_024446573.1:c.1684+101_1684+102del	XP_024302341.1:n.1684+101_1684+102del
XR_001743697.2:n.1715+101_1715+102del
XR_942606.2:n.1766+101_1766+102del
NM_032861.4:c.1684+101_1684+102del MANE Select	NP_116250.3:n.1684+101_1684+102del
NR_073096.2:n.1700_1701del