Canonical Allele Identifier: CA366254901

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535830G>T (hg19) ; chr6:g.158114798G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114798G>T , CM000668.2:g.158114798G>T	GRCh38
NC_000006.11:g.158535830G>T , CM000668.1:g.158535830G>T	GRCh37
NC_000006.10:g.158455818G>T	NCBI36
NG_032889.1:g.58483C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1395C>A	ENSP00000475855.1:n.*1395C>A
ENST00000642244.1:c.1585C>A	ENSP00000493554.1:p.Leu529Ile
ENST00000642903.1:c.1675C>A	ENSP00000493559.1:p.Leu559Ile
ENST00000644972.1:c.1675C>A	ENSP00000496451.1:p.Leu559Ile
ENST00000645077.1:c.*1296C>A	ENSP00000496113.1:n.*1296C>A
ENST00000645172.1:c.*1377C>A	ENSP00000495367.1:n.*1377C>A
ENST00000646190.1:n.3006C>A
ENST00000646208.1:c.1411C>A	ENSP00000493723.1:p.Leu471Ile
ENST00000646410.1:c.1546C>A	ENSP00000494205.1:p.Leu516Ile
ENST00000646562.1:c.*1509C>A	ENSP00000496087.1:n.*1509C>A
ENST00000647468.2:c.1675C>A MANE Select	ENSP00000496731.1:p.Leu559Ile
ENST00000648111.1:c.*1363C>A	ENSP00000497275.1:n.*1363C>A
ENST00000367101.5:c.*123C>A	ENSP00000356068.1:n.*123C>A
ENST00000367104.7:c.1675C>A	ENSP00000356071.3:p.Leu559Ile
ENST00000435180.5:c.400C>A	ENSP00000391168.1:p.Leu134Ile
ENST00000606965.5:c.*236C>A	ENSP00000475808.1:n.*236C>A
ENST00000607071.5:c.*1609C>A	ENSP00000475855.1:n.*1609C>A
ENST00000607742.5:c.*2953C>A	ENSP00000475523.1:n.*2953C>A
NM_032861.3:c.1675C>A	NP_116250.3:p.Leu559Ile
NR_073096.1:n.1608C>A
XM_006715586.1:c.1465C>A	XP_006715649.1:p.Leu489Ile
XM_011536196.1:c.1654C>A	XP_011534498.1:p.Leu552Ile
XM_011536197.1:c.1561C>A	XP_011534499.1:p.Leu521Ile
XM_011536198.1:c.1465C>A	XP_011534500.1:p.Leu489Ile
XM_006715586.3:c.1465C>A	XP_006715649.1:p.Leu489Ile
XM_011536196.3:c.1654C>A	XP_011534498.1:p.Leu552Ile
XM_011536198.3:c.1465C>A	XP_011534500.1:p.Leu489Ile
XM_024446573.1:c.1675C>A	XP_024302341.1:p.Leu559Ile
XR_001743697.2:n.1706C>A
XR_942606.2:n.1757C>A
NM_032861.4:c.1675C>A MANE Select	NP_116250.3:p.Leu559Ile
NR_073096.2:n.1590C>A