Canonical Allele Identifier: CA452820179

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535942G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114910G>A , CM000668.2:g.158114910G>A	GRCh38
NC_000006.11:g.158535942G>A , CM000668.1:g.158535942G>A	GRCh37
NC_000006.10:g.158455930G>A	NCBI36
NG_032889.1:g.58371C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.775C>T	ENSP00000391168.2:n.775C>T
ENST00000607071.6:c.*1283C>T	ENSP00000475855.1:n.*1283C>T
ENST00000642244.1:c.1473C>T	ENSP00000493554.1:p.Ile491=
ENST00000642903.1:c.1563C>T	ENSP00000493559.1:p.Ile521=
ENST00000644972.1:c.1563C>T	ENSP00000496451.1:p.Ile521=
ENST00000645077.1:c.*1184C>T	ENSP00000496113.1:n.*1184C>T
ENST00000645172.1:c.*1265C>T	ENSP00000495367.1:n.*1265C>T
ENST00000646190.1:n.2894C>T
ENST00000646208.1:c.1299C>T	ENSP00000493723.1:p.Ile433=
ENST00000646410.1:c.1434C>T	ENSP00000494205.1:p.Ile478=
ENST00000646562.1:c.*1397C>T	ENSP00000496087.1:n.*1397C>T
ENST00000647468.2:c.1563C>T MANE Select	ENSP00000496731.1:p.Ile521=
ENST00000648111.1:c.*1251C>T	ENSP00000497275.1:n.*1251C>T
ENST00000367101.5:c.*11C>T	ENSP00000356068.1:n.*11C>T
ENST00000367104.7:c.1563C>T	ENSP00000356071.3:p.Ile521=
ENST00000435180.5:c.288C>T	ENSP00000391168.1:p.Ile96=
ENST00000606965.5:c.*124C>T	ENSP00000475808.1:n.*124C>T
ENST00000607071.5:c.*1497C>T	ENSP00000475855.1:n.*1497C>T
ENST00000607742.5:c.*2841C>T	ENSP00000475523.1:n.*2841C>T
NM_032861.3:c.1563C>T	NP_116250.3:p.Ile521=
NR_073096.1:n.1496C>T
XM_006715586.1:c.1353C>T	XP_006715649.1:p.Ile451=
XM_011536196.1:c.1542C>T	XP_011534498.1:p.Ile514=
XM_011536197.1:c.1449C>T	XP_011534499.1:p.Ile483=
XM_011536198.1:c.1353C>T	XP_011534500.1:p.Ile451=
XM_006715586.3:c.1353C>T	XP_006715649.1:p.Ile451=
XM_011536196.3:c.1542C>T	XP_011534498.1:p.Ile514=
XM_011536198.3:c.1353C>T	XP_011534500.1:p.Ile451=
XM_024446573.1:c.1563C>T	XP_024302341.1:p.Ile521=
XR_001743697.2:n.1594C>T
XR_942606.2:n.1645C>T
NM_032861.4:c.1563C>T MANE Select	NP_116250.3:p.Ile521=
NR_073096.2:n.1478C>T