Canonical Allele Identifier: CA452822162

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567887C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146855C>G , CM000668.2:g.158146855C>G	GRCh38
NC_000006.11:g.158567887C>G , CM000668.1:g.158567887C>G	GRCh37
NC_000006.10:g.158487875C>G	NCBI36
NG_032889.1:g.26426G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*248G>C	ENSP00000475855.1:n.*248G>C
ENST00000642244.1:c.324G>C	ENSP00000493554.1:p.Arg108=
ENST00000642903.1:c.414G>C	ENSP00000493559.1:p.Arg138=
ENST00000644972.1:c.414G>C	ENSP00000496451.1:p.Arg138=
ENST00000645077.1:c.*248G>C	ENSP00000496113.1:n.*248G>C
ENST00000645172.1:c.*189+2010G>C	ENSP00000495367.1:n.*189+2010G>C
ENST00000646190.1:n.1645G>C
ENST00000646208.1:c.150G>C	ENSP00000493723.1:p.Arg50=
ENST00000646410.1:c.285G>C	ENSP00000494205.1:p.Arg95=
ENST00000646562.1:c.*248G>C	ENSP00000496087.1:n.*248G>C
ENST00000647468.2:c.414G>C MANE Select	ENSP00000496731.1:p.Arg138=
ENST00000648111.1:c.*58G>C	ENSP00000497275.1:n.*58G>C
ENST00000367101.5:c.414G>C	ENSP00000356068.1:p.Arg138=
ENST00000367104.7:c.414G>C	ENSP00000356071.3:p.Arg138=
ENST00000606965.5:c.414G>C	ENSP00000475808.1:p.Arg138=
ENST00000607000.1:c.414G>C	ENSP00000475788.1:p.Arg138=
ENST00000607071.5:c.*248G>C	ENSP00000475855.1:n.*248G>C
ENST00000607742.5:c.*248G>C	ENSP00000475523.1:n.*248G>C
NM_032861.3:c.414G>C	NP_116250.3:p.Arg138=
NR_073096.1:n.556G>C
XM_006715586.1:c.204G>C	XP_006715649.1:p.Arg68=
XM_011536196.1:c.393G>C	XP_011534498.1:p.Arg131=
XM_011536197.1:c.414G>C	XP_011534499.1:p.Arg138=
XM_011536198.1:c.204G>C	XP_011534500.1:p.Arg68=
XR_942606.1:n.415G>C
XM_006715586.3:c.204G>C	XP_006715649.1:p.Arg68=
XM_011536196.3:c.393G>C	XP_011534498.1:p.Arg131=
XM_011536198.3:c.204G>C	XP_011534500.1:p.Arg68=
XM_024446573.1:c.414G>C	XP_024302341.1:p.Arg138=
XR_001743697.2:n.495G>C
XR_942606.2:n.546G>C
NM_032861.4:c.414G>C MANE Select	NP_116250.3:p.Arg138=
NR_073096.2:n.538G>C