Canonical Allele Identifier: CA1096370108

Gene: SERAC1

Linked Data

• dbSNP Id: rs1784230745
• gnomAD v3: 6-158114567-TATTAAA-T
• gnomAD v4: 6-158114567-TATTAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114572_158114577del , CM000668.2:g.158114572_158114577del	GRCh38
NC_000006.11:g.158535604_158535609del , CM000668.1:g.158535604_158535609del	GRCh37
NC_000006.10:g.158455592_158455597del	NCBI36
NG_032889.1:g.58708_58713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+216_*1404+221del	ENSP00000475855.1:n.*1404+216_*1404+221del
ENST00000642244.1:c.1594+216_1594+221del	ENSP00000493554.1:n.1594+216_1594+221del
ENST00000644972.1:c.1684+216_1684+221del	ENSP00000496451.1:n.1684+216_1684+221del
ENST00000645077.1:c.*1305+216_*1305+221del	ENSP00000496113.1:n.*1305+216_*1305+221del
ENST00000645172.1:c.*1386+216_*1386+221del	ENSP00000495367.1:n.*1386+216_*1386+221del
ENST00000646190.1:n.3015+216_3015+221del
ENST00000646208.1:c.1420+216_1420+221del	ENSP00000493723.1:n.1420+216_1420+221del
ENST00000646410.1:c.1555+216_1555+221del	ENSP00000494205.1:n.1555+216_1555+221del
ENST00000646562.1:c.*1734_*1739del	ENSP00000496087.1:n.*1734_*1739del
ENST00000647468.2:c.1684+216_1684+221del MANE Select	ENSP00000496731.1:n.1684+216_1684+221del
ENST00000648111.1:c.*1372+216_*1372+221del	ENSP00000497275.1:n.*1372+216_*1372+221del
ENST00000367104.7:c.1684+216_1684+221del	ENSP00000356071.3:n.1684+216_1684+221del
ENST00000606965.5:c.*461_*466del	ENSP00000475808.1:n.*461_*466del
ENST00000607071.5:c.*1618+216_*1618+221del	ENSP00000475855.1:n.*1618+216_*1618+221del
ENST00000607742.5:c.*2962+216_*2962+221del	ENSP00000475523.1:n.*2962+216_*2962+221del
NM_032861.3:c.1684+216_1684+221del	NP_116250.3:n.1684+216_1684+221del
NR_073096.1:n.1833_1838del
XM_006715586.1:c.1474+216_1474+221del	XP_006715649.1:n.1474+216_1474+221del
XM_011536196.1:c.1663+216_1663+221del	XP_011534498.1:n.1663+216_1663+221del
XM_011536197.1:c.1570+216_1570+221del	XP_011534499.1:n.1570+216_1570+221del
XM_011536198.1:c.1474+216_1474+221del	XP_011534500.1:n.1474+216_1474+221del
XM_006715586.3:c.1474+216_1474+221del	XP_006715649.1:n.1474+216_1474+221del
XM_011536196.3:c.1663+216_1663+221del	XP_011534498.1:n.1663+216_1663+221del
XM_011536198.3:c.1474+216_1474+221del	XP_011534500.1:n.1474+216_1474+221del
XM_024446573.1:c.1684+216_1684+221del	XP_024302341.1:n.1684+216_1684+221del
XR_001743697.2:n.1715+216_1715+221del
XR_942606.2:n.1766+216_1766+221del
NM_032861.4:c.1684+216_1684+221del MANE Select	NP_116250.3:n.1684+216_1684+221del
NR_073096.2:n.1815_1820del