Canonical Allele Identifier: CA452820186

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535951A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114919A>G , CM000668.2:g.158114919A>G	GRCh38
NC_000006.11:g.158535951A>G , CM000668.1:g.158535951A>G	GRCh37
NC_000006.10:g.158455939A>G	NCBI36
NG_032889.1:g.58362T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.766T>C	ENSP00000391168.2:n.766T>C
ENST00000607071.6:c.*1274T>C	ENSP00000475855.1:n.*1274T>C
ENST00000642244.1:c.1464T>C	ENSP00000493554.1:p.Ser488=
ENST00000642903.1:c.1554T>C	ENSP00000493559.1:p.Ser518=
ENST00000644972.1:c.1554T>C	ENSP00000496451.1:p.Ser518=
ENST00000645077.1:c.*1175T>C	ENSP00000496113.1:n.*1175T>C
ENST00000645172.1:c.*1256T>C	ENSP00000495367.1:n.*1256T>C
ENST00000646190.1:n.2885T>C
ENST00000646208.1:c.1290T>C	ENSP00000493723.1:p.Ser430=
ENST00000646410.1:c.1425T>C	ENSP00000494205.1:p.Ser475=
ENST00000646562.1:c.*1388T>C	ENSP00000496087.1:n.*1388T>C
ENST00000647468.2:c.1554T>C MANE Select	ENSP00000496731.1:p.Ser518=
ENST00000648111.1:c.*1242T>C	ENSP00000497275.1:n.*1242T>C
ENST00000367101.5:c.*2T>C	ENSP00000356068.1:n.*2T>C
ENST00000367104.7:c.1554T>C	ENSP00000356071.3:p.Ser518=
ENST00000435180.5:c.279T>C	ENSP00000391168.1:p.Ser93=
ENST00000606965.5:c.*115T>C	ENSP00000475808.1:n.*115T>C
ENST00000607071.5:c.*1488T>C	ENSP00000475855.1:n.*1488T>C
ENST00000607742.5:c.*2832T>C	ENSP00000475523.1:n.*2832T>C
NM_032861.3:c.1554T>C	NP_116250.3:p.Ser518=
NR_073096.1:n.1487T>C
XM_006715586.1:c.1344T>C	XP_006715649.1:p.Ser448=
XM_011536196.1:c.1533T>C	XP_011534498.1:p.Ser511=
XM_011536197.1:c.1440T>C	XP_011534499.1:p.Ser480=
XM_011536198.1:c.1344T>C	XP_011534500.1:p.Ser448=
XM_006715586.3:c.1344T>C	XP_006715649.1:p.Ser448=
XM_011536196.3:c.1533T>C	XP_011534498.1:p.Ser511=
XM_011536198.3:c.1344T>C	XP_011534500.1:p.Ser448=
XM_024446573.1:c.1554T>C	XP_024302341.1:p.Ser518=
XR_001743697.2:n.1585T>C
XR_942606.2:n.1636T>C
NM_032861.4:c.1554T>C MANE Select	NP_116250.3:p.Ser518=
NR_073096.2:n.1469T>C