Canonical Allele Identifier: CA821386361

Gene: SERAC1

Linked Data

• dbSNP Id: rs1332210776
• gnomAD v3: 6-158114724-T-TC
• gnomAD v4: 6-158114724-T-TC
• MyVariant Identifiers: chr6:g.158535756_158535757insC (hg19) ; chr6:g.158114724_158114725insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114724_158114725insC , CM000668.2:g.158114724_158114725insC	GRCh38
NC_000006.11:g.158535756_158535757insC , CM000668.1:g.158535756_158535757insC	GRCh37
NC_000006.10:g.158455744_158455745insC	NCBI36
NG_032889.1:g.58556_58557insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+64_*1404+65insG	ENSP00000475855.1:n.*1404+64_*1404+65insG
ENST00000642244.1:c.1594+64_1594+65insG	ENSP00000493554.1:n.1594+64_1594+65insG
ENST00000642903.1:c.1748_1749insG	ENSP00000493559.1:p.Phe585ValfsTer15
ENST00000644972.1:c.1684+64_1684+65insG	ENSP00000496451.1:n.1684+64_1684+65insG
ENST00000645077.1:c.*1305+64_*1305+65insG	ENSP00000496113.1:n.*1305+64_*1305+65insG
ENST00000645172.1:c.*1386+64_*1386+65insG	ENSP00000495367.1:n.*1386+64_*1386+65insG
ENST00000646190.1:n.3015+64_3015+65insG
ENST00000646208.1:c.1420+64_1420+65insG	ENSP00000493723.1:n.1420+64_1420+65insG
ENST00000646410.1:c.1555+64_1555+65insG	ENSP00000494205.1:n.1555+64_1555+65insG
ENST00000646562.1:c.*1582_*1583insG	ENSP00000496087.1:n.*1582_*1583insG
ENST00000647468.2:c.1684+64_1684+65insG MANE Select	ENSP00000496731.1:n.1684+64_1684+65insG
ENST00000648111.1:c.*1372+64_*1372+65insG	ENSP00000497275.1:n.*1372+64_*1372+65insG
ENST00000367104.7:c.1684+64_1684+65insG	ENSP00000356071.3:n.1684+64_1684+65insG
ENST00000435180.5:c.473_474insG	ENSP00000391168.1:p.Phe160ValfsTer?
ENST00000606965.5:c.*309_*310insG	ENSP00000475808.1:n.*309_*310insG
ENST00000607071.5:c.*1618+64_*1618+65insG	ENSP00000475855.1:n.*1618+64_*1618+65insG
ENST00000607742.5:c.*2962+64_*2962+65insG	ENSP00000475523.1:n.*2962+64_*2962+65insG
NM_032861.3:c.1684+64_1684+65insG	NP_116250.3:n.1684+64_1684+65insG
NR_073096.1:n.1681_1682insG
XM_006715586.1:c.1474+64_1474+65insG	XP_006715649.1:n.1474+64_1474+65insG
XM_011536196.1:c.1663+64_1663+65insG	XP_011534498.1:n.1663+64_1663+65insG
XM_011536197.1:c.1570+64_1570+65insG	XP_011534499.1:n.1570+64_1570+65insG
XM_011536198.1:c.1474+64_1474+65insG	XP_011534500.1:n.1474+64_1474+65insG
XM_006715586.3:c.1474+64_1474+65insG	XP_006715649.1:n.1474+64_1474+65insG
XM_011536196.3:c.1663+64_1663+65insG	XP_011534498.1:n.1663+64_1663+65insG
XM_011536198.3:c.1474+64_1474+65insG	XP_011534500.1:n.1474+64_1474+65insG
XM_024446573.1:c.1684+64_1684+65insG	XP_024302341.1:n.1684+64_1684+65insG
XR_001743697.2:n.1715+64_1715+65insG
XR_942606.2:n.1766+64_1766+65insG
NM_032861.4:c.1684+64_1684+65insG MANE Select	NP_116250.3:n.1684+64_1684+65insG
NR_073096.2:n.1663_1664insG