Canonical Allele Identifier: CA452820091

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535864G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114832G>C , CM000668.2:g.158114832G>C	GRCh38
NC_000006.11:g.158535864G>C , CM000668.1:g.158535864G>C	GRCh37
NC_000006.10:g.158455852G>C	NCBI36
NG_032889.1:g.58449C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.853C>G	ENSP00000391168.2:n.853C>G
ENST00000607071.6:c.*1361C>G	ENSP00000475855.1:n.*1361C>G
ENST00000642244.1:c.1551C>G	ENSP00000493554.1:p.Arg517=
ENST00000642903.1:c.1641C>G	ENSP00000493559.1:p.Arg547=
ENST00000644972.1:c.1641C>G	ENSP00000496451.1:p.Arg547=
ENST00000645077.1:c.*1262C>G	ENSP00000496113.1:n.*1262C>G
ENST00000645172.1:c.*1343C>G	ENSP00000495367.1:n.*1343C>G
ENST00000646190.1:n.2972C>G
ENST00000646208.1:c.1377C>G	ENSP00000493723.1:p.Arg459=
ENST00000646410.1:c.1512C>G	ENSP00000494205.1:p.Arg504=
ENST00000646562.1:c.*1475C>G	ENSP00000496087.1:n.*1475C>G
ENST00000647468.2:c.1641C>G MANE Select	ENSP00000496731.1:p.Arg547=
ENST00000648111.1:c.*1329C>G	ENSP00000497275.1:n.*1329C>G
ENST00000367101.5:c.*89C>G	ENSP00000356068.1:n.*89C>G
ENST00000367104.7:c.1641C>G	ENSP00000356071.3:p.Arg547=
ENST00000435180.5:c.366C>G	ENSP00000391168.1:p.Arg122=
ENST00000606965.5:c.*202C>G	ENSP00000475808.1:n.*202C>G
ENST00000607071.5:c.*1575C>G	ENSP00000475855.1:n.*1575C>G
ENST00000607742.5:c.*2919C>G	ENSP00000475523.1:n.*2919C>G
NM_032861.3:c.1641C>G	NP_116250.3:p.Arg547=
NR_073096.1:n.1574C>G
XM_006715586.1:c.1431C>G	XP_006715649.1:p.Arg477=
XM_011536196.1:c.1620C>G	XP_011534498.1:p.Arg540=
XM_011536197.1:c.1527C>G	XP_011534499.1:p.Arg509=
XM_011536198.1:c.1431C>G	XP_011534500.1:p.Arg477=
XM_006715586.3:c.1431C>G	XP_006715649.1:p.Arg477=
XM_011536196.3:c.1620C>G	XP_011534498.1:p.Arg540=
XM_011536198.3:c.1431C>G	XP_011534500.1:p.Arg477=
XM_024446573.1:c.1641C>G	XP_024302341.1:p.Arg547=
XR_001743697.2:n.1672C>G
XR_942606.2:n.1723C>G
NM_032861.4:c.1641C>G MANE Select	NP_116250.3:p.Arg547=
NR_073096.2:n.1556C>G