Canonical Allele Identifier: CA366255107

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114894-T-C
• MyVariant Identifiers: chr6:g.158535926T>C (hg19) ; chr6:g.158114894T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114894T>C , CM000668.2:g.158114894T>C	GRCh38
NC_000006.11:g.158535926T>C , CM000668.1:g.158535926T>C	GRCh37
NC_000006.10:g.158455914T>C	NCBI36
NG_032889.1:g.58387A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.791A>G	ENSP00000391168.2:n.791A>G
ENST00000607071.6:c.*1299A>G	ENSP00000475855.1:n.*1299A>G
ENST00000642244.1:c.1489A>G	ENSP00000493554.1:p.Ile497Val
ENST00000642903.1:c.1579A>G	ENSP00000493559.1:p.Ile527Val
ENST00000644972.1:c.1579A>G	ENSP00000496451.1:p.Ile527Val
ENST00000645077.1:c.*1200A>G	ENSP00000496113.1:n.*1200A>G
ENST00000645172.1:c.*1281A>G	ENSP00000495367.1:n.*1281A>G
ENST00000646190.1:n.2910A>G
ENST00000646208.1:c.1315A>G	ENSP00000493723.1:p.Ile439Val
ENST00000646410.1:c.1450A>G	ENSP00000494205.1:p.Ile484Val
ENST00000646562.1:c.*1413A>G	ENSP00000496087.1:n.*1413A>G
ENST00000647468.2:c.1579A>G MANE Select	ENSP00000496731.1:p.Ile527Val
ENST00000648111.1:c.*1267A>G	ENSP00000497275.1:n.*1267A>G
ENST00000367101.5:c.*27A>G	ENSP00000356068.1:n.*27A>G
ENST00000367104.7:c.1579A>G	ENSP00000356071.3:p.Ile527Val
ENST00000435180.5:c.304A>G	ENSP00000391168.1:p.Ile102Val
ENST00000606965.5:c.*140A>G	ENSP00000475808.1:n.*140A>G
ENST00000607071.5:c.*1513A>G	ENSP00000475855.1:n.*1513A>G
ENST00000607742.5:c.*2857A>G	ENSP00000475523.1:n.*2857A>G
NM_032861.3:c.1579A>G	NP_116250.3:p.Ile527Val
NR_073096.1:n.1512A>G
XM_006715586.1:c.1369A>G	XP_006715649.1:p.Ile457Val
XM_011536196.1:c.1558A>G	XP_011534498.1:p.Ile520Val
XM_011536197.1:c.1465A>G	XP_011534499.1:p.Ile489Val
XM_011536198.1:c.1369A>G	XP_011534500.1:p.Ile457Val
XM_006715586.3:c.1369A>G	XP_006715649.1:p.Ile457Val
XM_011536196.3:c.1558A>G	XP_011534498.1:p.Ile520Val
XM_011536198.3:c.1369A>G	XP_011534500.1:p.Ile457Val
XM_024446573.1:c.1579A>G	XP_024302341.1:p.Ile527Val
XR_001743697.2:n.1610A>G
XR_942606.2:n.1661A>G
NM_032861.4:c.1579A>G MANE Select	NP_116250.3:p.Ile527Val
NR_073096.2:n.1494A>G