Canonical Allele Identifier: CA366255299

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158536000A>T (hg19) ; chr6:g.158114968A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114968A>T , CM000668.2:g.158114968A>T	GRCh38
NC_000006.11:g.158536000A>T , CM000668.1:g.158536000A>T	GRCh37
NC_000006.10:g.158455988A>T	NCBI36
NG_032889.1:g.58313T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.717T>A	ENSP00000391168.2:n.717T>A
ENST00000607071.6:c.*1225T>A	ENSP00000475855.1:n.*1225T>A
ENST00000642244.1:c.1415T>A	ENSP00000493554.1:p.Leu472His
ENST00000642903.1:c.1505T>A	ENSP00000493559.1:p.Leu502His
ENST00000644972.1:c.1505T>A	ENSP00000496451.1:p.Leu502His
ENST00000645077.1:c.*1126T>A	ENSP00000496113.1:n.*1126T>A
ENST00000645172.1:c.*1207T>A	ENSP00000495367.1:n.*1207T>A
ENST00000646190.1:n.2836T>A
ENST00000646208.1:c.1241T>A	ENSP00000493723.1:p.Leu414His
ENST00000646410.1:c.1376T>A	ENSP00000494205.1:p.Leu459His
ENST00000646562.1:c.*1339T>A	ENSP00000496087.1:n.*1339T>A
ENST00000647468.2:c.1505T>A MANE Select	ENSP00000496731.1:p.Leu502His
ENST00000648111.1:c.*1193T>A	ENSP00000497275.1:n.*1193T>A
ENST00000367101.5:c.1549T>A	ENSP00000356068.1:p.Phe517Ile
ENST00000367104.7:c.1505T>A	ENSP00000356071.3:p.Leu502His
ENST00000435180.5:c.230T>A	ENSP00000391168.1:p.Leu77His
ENST00000606965.5:c.*66T>A	ENSP00000475808.1:n.*66T>A
ENST00000607071.5:c.*1439T>A	ENSP00000475855.1:n.*1439T>A
ENST00000607742.5:c.*2783T>A	ENSP00000475523.1:n.*2783T>A
NM_032861.3:c.1505T>A	NP_116250.3:p.Leu502His
NR_073096.1:n.1438T>A
XM_006715586.1:c.1295T>A	XP_006715649.1:p.Leu432His
XM_011536196.1:c.1484T>A	XP_011534498.1:p.Leu495His
XM_011536197.1:c.1391T>A	XP_011534499.1:p.Leu464His
XM_011536198.1:c.1295T>A	XP_011534500.1:p.Leu432His
XM_006715586.3:c.1295T>A	XP_006715649.1:p.Leu432His
XM_011536196.3:c.1484T>A	XP_011534498.1:p.Leu495His
XM_011536198.3:c.1295T>A	XP_011534500.1:p.Leu432His
XM_024446573.1:c.1505T>A	XP_024302341.1:p.Leu502His
XR_001743697.2:n.1536T>A
XR_942606.2:n.1587T>A
NM_032861.4:c.1505T>A MANE Select	NP_116250.3:p.Leu502His
NR_073096.2:n.1420T>A