Canonical Allele Identifier: CA366255010

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535882T>A (hg19) ; chr6:g.158114850T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114850T>A , CM000668.2:g.158114850T>A	GRCh38
NC_000006.11:g.158535882T>A , CM000668.1:g.158535882T>A	GRCh37
NC_000006.10:g.158455870T>A	NCBI36
NG_032889.1:g.58431A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.835A>T	ENSP00000391168.2:n.835A>T
ENST00000607071.6:c.*1343A>T	ENSP00000475855.1:n.*1343A>T
ENST00000642244.1:c.1533A>T	ENSP00000493554.1:p.Glu511Asp
ENST00000642903.1:c.1623A>T	ENSP00000493559.1:p.Glu541Asp
ENST00000644972.1:c.1623A>T	ENSP00000496451.1:p.Glu541Asp
ENST00000645077.1:c.*1244A>T	ENSP00000496113.1:n.*1244A>T
ENST00000645172.1:c.*1325A>T	ENSP00000495367.1:n.*1325A>T
ENST00000646190.1:n.2954A>T
ENST00000646208.1:c.1359A>T	ENSP00000493723.1:p.Glu453Asp
ENST00000646410.1:c.1494A>T	ENSP00000494205.1:p.Glu498Asp
ENST00000646562.1:c.*1457A>T	ENSP00000496087.1:n.*1457A>T
ENST00000647468.2:c.1623A>T MANE Select	ENSP00000496731.1:p.Glu541Asp
ENST00000648111.1:c.*1311A>T	ENSP00000497275.1:n.*1311A>T
ENST00000367101.5:c.*71A>T	ENSP00000356068.1:n.*71A>T
ENST00000367104.7:c.1623A>T	ENSP00000356071.3:p.Glu541Asp
ENST00000435180.5:c.348A>T	ENSP00000391168.1:p.Glu116Asp
ENST00000606965.5:c.*184A>T	ENSP00000475808.1:n.*184A>T
ENST00000607071.5:c.*1557A>T	ENSP00000475855.1:n.*1557A>T
ENST00000607742.5:c.*2901A>T	ENSP00000475523.1:n.*2901A>T
NM_032861.3:c.1623A>T	NP_116250.3:p.Glu541Asp
NR_073096.1:n.1556A>T
XM_006715586.1:c.1413A>T	XP_006715649.1:p.Glu471Asp
XM_011536196.1:c.1602A>T	XP_011534498.1:p.Glu534Asp
XM_011536197.1:c.1509A>T	XP_011534499.1:p.Glu503Asp
XM_011536198.1:c.1413A>T	XP_011534500.1:p.Glu471Asp
XM_006715586.3:c.1413A>T	XP_006715649.1:p.Glu471Asp
XM_011536196.3:c.1602A>T	XP_011534498.1:p.Glu534Asp
XM_011536198.3:c.1413A>T	XP_011534500.1:p.Glu471Asp
XM_024446573.1:c.1623A>T	XP_024302341.1:p.Glu541Asp
XR_001743697.2:n.1654A>T
XR_942606.2:n.1705A>T
NM_032861.4:c.1623A>T MANE Select	NP_116250.3:p.Glu541Asp
NR_073096.2:n.1538A>T