Canonical Allele Identifier: CA366254904

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535832T>A (hg19) ; chr6:g.158114800T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114800T>A , CM000668.2:g.158114800T>A	GRCh38
NC_000006.11:g.158535832T>A , CM000668.1:g.158535832T>A	GRCh37
NC_000006.10:g.158455820T>A	NCBI36
NG_032889.1:g.58481A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1393A>T	ENSP00000475855.1:n.*1393A>T
ENST00000642244.1:c.1583A>T	ENSP00000493554.1:p.Glu528Val
ENST00000642903.1:c.1673A>T	ENSP00000493559.1:p.Glu558Val
ENST00000644972.1:c.1673A>T	ENSP00000496451.1:p.Glu558Val
ENST00000645077.1:c.*1294A>T	ENSP00000496113.1:n.*1294A>T
ENST00000645172.1:c.*1375A>T	ENSP00000495367.1:n.*1375A>T
ENST00000646190.1:n.3004A>T
ENST00000646208.1:c.1409A>T	ENSP00000493723.1:p.Glu470Val
ENST00000646410.1:c.1544A>T	ENSP00000494205.1:p.Glu515Val
ENST00000646562.1:c.*1507A>T	ENSP00000496087.1:n.*1507A>T
ENST00000647468.2:c.1673A>T MANE Select	ENSP00000496731.1:p.Glu558Val
ENST00000648111.1:c.*1361A>T	ENSP00000497275.1:n.*1361A>T
ENST00000367101.5:c.*121A>T	ENSP00000356068.1:n.*121A>T
ENST00000367104.7:c.1673A>T	ENSP00000356071.3:p.Glu558Val
ENST00000435180.5:c.398A>T	ENSP00000391168.1:p.Glu133Val
ENST00000606965.5:c.*234A>T	ENSP00000475808.1:n.*234A>T
ENST00000607071.5:c.*1607A>T	ENSP00000475855.1:n.*1607A>T
ENST00000607742.5:c.*2951A>T	ENSP00000475523.1:n.*2951A>T
NM_032861.3:c.1673A>T	NP_116250.3:p.Glu558Val
NR_073096.1:n.1606A>T
XM_006715586.1:c.1463A>T	XP_006715649.1:p.Glu488Val
XM_011536196.1:c.1652A>T	XP_011534498.1:p.Glu551Val
XM_011536197.1:c.1559A>T	XP_011534499.1:p.Glu520Val
XM_011536198.1:c.1463A>T	XP_011534500.1:p.Glu488Val
XM_006715586.3:c.1463A>T	XP_006715649.1:p.Glu488Val
XM_011536196.3:c.1652A>T	XP_011534498.1:p.Glu551Val
XM_011536198.3:c.1463A>T	XP_011534500.1:p.Glu488Val
XM_024446573.1:c.1673A>T	XP_024302341.1:p.Glu558Val
XR_001743697.2:n.1704A>T
XR_942606.2:n.1755A>T
NM_032861.4:c.1673A>T MANE Select	NP_116250.3:p.Glu558Val
NR_073096.2:n.1588A>T