Canonical Allele Identifier: CA366255160

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535950T>C (hg19) ; chr6:g.158114918T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114918T>C , CM000668.2:g.158114918T>C	GRCh38
NC_000006.11:g.158535950T>C , CM000668.1:g.158535950T>C	GRCh37
NC_000006.10:g.158455938T>C	NCBI36
NG_032889.1:g.58363A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.767A>G	ENSP00000391168.2:n.767A>G
ENST00000607071.6:c.*1275A>G	ENSP00000475855.1:n.*1275A>G
ENST00000642244.1:c.1465A>G	ENSP00000493554.1:p.Thr489Ala
ENST00000642903.1:c.1555A>G	ENSP00000493559.1:p.Thr519Ala
ENST00000644972.1:c.1555A>G	ENSP00000496451.1:p.Thr519Ala
ENST00000645077.1:c.*1176A>G	ENSP00000496113.1:n.*1176A>G
ENST00000645172.1:c.*1257A>G	ENSP00000495367.1:n.*1257A>G
ENST00000646190.1:n.2886A>G
ENST00000646208.1:c.1291A>G	ENSP00000493723.1:p.Thr431Ala
ENST00000646410.1:c.1426A>G	ENSP00000494205.1:p.Thr476Ala
ENST00000646562.1:c.*1389A>G	ENSP00000496087.1:n.*1389A>G
ENST00000647468.2:c.1555A>G MANE Select	ENSP00000496731.1:p.Thr519Ala
ENST00000648111.1:c.*1243A>G	ENSP00000497275.1:n.*1243A>G
ENST00000367101.5:c.*3A>G	ENSP00000356068.1:n.*3A>G
ENST00000367104.7:c.1555A>G	ENSP00000356071.3:p.Thr519Ala
ENST00000435180.5:c.280A>G	ENSP00000391168.1:p.Thr94Ala
ENST00000606965.5:c.*116A>G	ENSP00000475808.1:n.*116A>G
ENST00000607071.5:c.*1489A>G	ENSP00000475855.1:n.*1489A>G
ENST00000607742.5:c.*2833A>G	ENSP00000475523.1:n.*2833A>G
NM_032861.3:c.1555A>G	NP_116250.3:p.Thr519Ala
NR_073096.1:n.1488A>G
XM_006715586.1:c.1345A>G	XP_006715649.1:p.Thr449Ala
XM_011536196.1:c.1534A>G	XP_011534498.1:p.Thr512Ala
XM_011536197.1:c.1441A>G	XP_011534499.1:p.Thr481Ala
XM_011536198.1:c.1345A>G	XP_011534500.1:p.Thr449Ala
XM_006715586.3:c.1345A>G	XP_006715649.1:p.Thr449Ala
XM_011536196.3:c.1534A>G	XP_011534498.1:p.Thr512Ala
XM_011536198.3:c.1345A>G	XP_011534500.1:p.Thr449Ala
XM_024446573.1:c.1555A>G	XP_024302341.1:p.Thr519Ala
XR_001743697.2:n.1586A>G
XR_942606.2:n.1637A>G
NM_032861.4:c.1555A>G MANE Select	NP_116250.3:p.Thr519Ala
NR_073096.2:n.1470A>G