Canonical Allele Identifier: CA150914300

Gene: SERAC1

Linked Data

• dbSNP Id: rs990744999
• gnomAD v2: 6-158535593-A-AGAT
• gnomAD v3: 6-158114561-A-AGAT
• gnomAD v4: 6-158114561-A-AGAT
• MyVariant Identifiers: chr6:g.158535593_158535594insGAT (hg19) ; chr6:g.158114561_158114562insGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114562_158114564dup , CM000668.2:g.158114562_158114564dup	GRCh38
NC_000006.11:g.158535594_158535596dup , CM000668.1:g.158535594_158535596dup	GRCh37
NC_000006.10:g.158455582_158455584dup	NCBI36
NG_032889.1:g.58717_58719dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+225_*1404+227dup	ENSP00000475855.1:n.*1404+225_*1404+227dup
ENST00000642244.1:c.1594+225_1594+227dup	ENSP00000493554.1:n.1594+225_1594+227dup
ENST00000644972.1:c.1684+225_1684+227dup	ENSP00000496451.1:n.1684+225_1684+227dup
ENST00000645077.1:c.*1305+225_*1305+227dup	ENSP00000496113.1:n.*1305+225_*1305+227dup
ENST00000645172.1:c.*1386+225_*1386+227dup	ENSP00000495367.1:n.*1386+225_*1386+227dup
ENST00000646190.1:n.3015+225_3015+227dup
ENST00000646208.1:c.1420+225_1420+227dup	ENSP00000493723.1:n.1420+225_1420+227dup
ENST00000646410.1:c.1555+225_1555+227dup	ENSP00000494205.1:n.1555+225_1555+227dup
ENST00000646562.1:c.*1743_*1745dup	ENSP00000496087.1:n.*1743_*1745dup
ENST00000647468.2:c.1684+225_1684+227dup MANE Select	ENSP00000496731.1:n.1684+225_1684+227dup
ENST00000648111.1:c.*1372+225_*1372+227dup	ENSP00000497275.1:n.*1372+225_*1372+227dup
ENST00000367104.7:c.1684+225_1684+227dup	ENSP00000356071.3:n.1684+225_1684+227dup
ENST00000606965.5:c.*470_*472dup	ENSP00000475808.1:n.*470_*472dup
ENST00000607071.5:c.*1618+225_*1618+227dup	ENSP00000475855.1:n.*1618+225_*1618+227dup
ENST00000607742.5:c.*2962+225_*2962+227dup	ENSP00000475523.1:n.*2962+225_*2962+227dup
NM_032861.3:c.1684+225_1684+227dup	NP_116250.3:n.1684+225_1684+227dup
NR_073096.1:n.1842_1844dup
XM_006715586.1:c.1474+225_1474+227dup	XP_006715649.1:n.1474+225_1474+227dup
XM_011536196.1:c.1663+225_1663+227dup	XP_011534498.1:n.1663+225_1663+227dup
XM_011536197.1:c.1570+225_1570+227dup	XP_011534499.1:n.1570+225_1570+227dup
XM_011536198.1:c.1474+225_1474+227dup	XP_011534500.1:n.1474+225_1474+227dup
XM_006715586.3:c.1474+225_1474+227dup	XP_006715649.1:n.1474+225_1474+227dup
XM_011536196.3:c.1663+225_1663+227dup	XP_011534498.1:n.1663+225_1663+227dup
XM_011536198.3:c.1474+225_1474+227dup	XP_011534500.1:n.1474+225_1474+227dup
XM_024446573.1:c.1684+225_1684+227dup	XP_024302341.1:n.1684+225_1684+227dup
XR_001743697.2:n.1715+225_1715+227dup
XR_942606.2:n.1766+225_1766+227dup
NM_032861.4:c.1684+225_1684+227dup MANE Select	NP_116250.3:n.1684+225_1684+227dup
NR_073096.2:n.1824_1826dup