Canonical Allele Identifier: CA150914713

Gene: SERAC1

Linked Data

• dbSNP Id: rs1040731884
• gnomAD v2: 6-158535775-C-CTGA
• gnomAD v3: 6-158114743-C-CTGA
• gnomAD v4: 6-158114743-C-CTGA
• MyVariant Identifiers: chr6:g.158535775_158535776insTGA (hg19) ; chr6:g.158114743_158114744insTGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114746_158114748dup , CM000668.2:g.158114746_158114748dup	GRCh38
NC_000006.11:g.158535778_158535780dup , CM000668.1:g.158535778_158535780dup	GRCh37
NC_000006.10:g.158455766_158455768dup	NCBI36
NG_032889.1:g.58535_58537dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000607071.6:c.*1404+43_*1404+45dup	ENSP00000475855.1:n.*1404+43_*1404+45dup
ENST00000642244.1:c.1594+43_1594+45dup	ENSP00000493554.1:n.1594+43_1594+45dup
ENST00000642903.1:c.1727_1729dup	ENSP00000493559.1:p.Ile576_Ser577insIle
ENST00000644972.1:c.1684+43_1684+45dup	ENSP00000496451.1:n.1684+43_1684+45dup
ENST00000645077.1:c.*1305+43_*1305+45dup	ENSP00000496113.1:n.*1305+43_*1305+45dup
ENST00000645172.1:c.*1386+43_*1386+45dup	ENSP00000495367.1:n.*1386+43_*1386+45dup
ENST00000646190.1:n.3015+43_3015+45dup
ENST00000646208.1:c.1420+43_1420+45dup	ENSP00000493723.1:n.1420+43_1420+45dup
ENST00000646410.1:c.1555+43_1555+45dup	ENSP00000494205.1:n.1555+43_1555+45dup
ENST00000646562.1:c.*1561_*1563dup	ENSP00000496087.1:n.*1561_*1563dup
ENST00000647468.2:c.1684+43_1684+45dup MANE Select	ENSP00000496731.1:n.1684+43_1684+45dup
ENST00000648111.1:c.*1372+43_*1372+45dup	ENSP00000497275.1:n.*1372+43_*1372+45dup
ENST00000367101.5:c.*175_*177dup	ENSP00000356068.1:n.*175_*177dup
ENST00000367104.7:c.1684+43_1684+45dup	ENSP00000356071.3:n.1684+43_1684+45dup
ENST00000435180.5:c.452_454dup	ENSP00000391168.1:p.Ile151_Ser152insIle
ENST00000606965.5:c.*288_*290dup	ENSP00000475808.1:n.*288_*290dup
ENST00000607071.5:c.*1618+43_*1618+45dup	ENSP00000475855.1:n.*1618+43_*1618+45dup
ENST00000607742.5:c.*2962+43_*2962+45dup	ENSP00000475523.1:n.*2962+43_*2962+45dup
NM_032861.3:c.1684+43_1684+45dup	NP_116250.3:n.1684+43_1684+45dup
NR_073096.1:n.1660_1662dup
XM_006715586.1:c.1474+43_1474+45dup	XP_006715649.1:n.1474+43_1474+45dup
XM_011536196.1:c.1663+43_1663+45dup	XP_011534498.1:n.1663+43_1663+45dup
XM_011536197.1:c.1570+43_1570+45dup	XP_011534499.1:n.1570+43_1570+45dup
XM_011536198.1:c.1474+43_1474+45dup	XP_011534500.1:n.1474+43_1474+45dup
XM_006715586.3:c.1474+43_1474+45dup	XP_006715649.1:n.1474+43_1474+45dup
XM_011536196.3:c.1663+43_1663+45dup	XP_011534498.1:n.1663+43_1663+45dup
XM_011536198.3:c.1474+43_1474+45dup	XP_011534500.1:n.1474+43_1474+45dup
XM_024446573.1:c.1684+43_1684+45dup	XP_024302341.1:n.1684+43_1684+45dup
XR_001743697.2:n.1715+43_1715+45dup
XR_942606.2:n.1766+43_1766+45dup
NM_032861.4:c.1684+43_1684+45dup MANE Select	NP_116250.3:n.1684+43_1684+45dup
NR_073096.2:n.1642_1644dup