Canonical Allele Identifier: CA452820066

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535828G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114796G>T , CM000668.2:g.158114796G>T	GRCh38
NC_000006.11:g.158535828G>T , CM000668.1:g.158535828G>T	GRCh37
NC_000006.10:g.158455816G>T	NCBI36
NG_032889.1:g.58485C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1397C>A	ENSP00000475855.1:n.*1397C>A
ENST00000642244.1:c.1587C>A	ENSP00000493554.1:p.Leu529=
ENST00000642903.1:c.1677C>A	ENSP00000493559.1:p.Leu559=
ENST00000644972.1:c.1677C>A	ENSP00000496451.1:p.Leu559=
ENST00000645077.1:c.*1298C>A	ENSP00000496113.1:n.*1298C>A
ENST00000645172.1:c.*1379C>A	ENSP00000495367.1:n.*1379C>A
ENST00000646190.1:n.3008C>A
ENST00000646208.1:c.1413C>A	ENSP00000493723.1:p.Leu471=
ENST00000646410.1:c.1548C>A	ENSP00000494205.1:p.Leu516=
ENST00000646562.1:c.*1511C>A	ENSP00000496087.1:n.*1511C>A
ENST00000647468.2:c.1677C>A MANE Select	ENSP00000496731.1:p.Leu559=
ENST00000648111.1:c.*1365C>A	ENSP00000497275.1:n.*1365C>A
ENST00000367101.5:c.*125C>A	ENSP00000356068.1:n.*125C>A
ENST00000367104.7:c.1677C>A	ENSP00000356071.3:p.Leu559=
ENST00000435180.5:c.402C>A	ENSP00000391168.1:p.Leu134=
ENST00000606965.5:c.*238C>A	ENSP00000475808.1:n.*238C>A
ENST00000607071.5:c.*1611C>A	ENSP00000475855.1:n.*1611C>A
ENST00000607742.5:c.*2955C>A	ENSP00000475523.1:n.*2955C>A
NM_032861.3:c.1677C>A	NP_116250.3:p.Leu559=
NR_073096.1:n.1610C>A
XM_006715586.1:c.1467C>A	XP_006715649.1:p.Leu489=
XM_011536196.1:c.1656C>A	XP_011534498.1:p.Leu552=
XM_011536197.1:c.1563C>A	XP_011534499.1:p.Leu521=
XM_011536198.1:c.1467C>A	XP_011534500.1:p.Leu489=
XM_006715586.3:c.1467C>A	XP_006715649.1:p.Leu489=
XM_011536196.3:c.1656C>A	XP_011534498.1:p.Leu552=
XM_011536198.3:c.1467C>A	XP_011534500.1:p.Leu489=
XM_024446573.1:c.1677C>A	XP_024302341.1:p.Leu559=
XR_001743697.2:n.1708C>A
XR_942606.2:n.1759C>A
NM_032861.4:c.1677C>A MANE Select	NP_116250.3:p.Leu559=
NR_073096.2:n.1592C>A