Canonical Allele Identifier: CA366254951

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114822-A-C
• MyVariant Identifiers: chr6:g.158535854A>C (hg19) ; chr6:g.158114822A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114822A>C , CM000668.2:g.158114822A>C	GRCh38
NC_000006.11:g.158535854A>C , CM000668.1:g.158535854A>C	GRCh37
NC_000006.10:g.158455842A>C	NCBI36
NG_032889.1:g.58459T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1371T>G	ENSP00000475855.1:n.*1371T>G
ENST00000642244.1:c.1561T>G	ENSP00000493554.1:p.Phe521Val
ENST00000642903.1:c.1651T>G	ENSP00000493559.1:p.Phe551Val
ENST00000644972.1:c.1651T>G	ENSP00000496451.1:p.Phe551Val
ENST00000645077.1:c.*1272T>G	ENSP00000496113.1:n.*1272T>G
ENST00000645172.1:c.*1353T>G	ENSP00000495367.1:n.*1353T>G
ENST00000646190.1:n.2982T>G
ENST00000646208.1:c.1387T>G	ENSP00000493723.1:p.Phe463Val
ENST00000646410.1:c.1522T>G	ENSP00000494205.1:p.Phe508Val
ENST00000646562.1:c.*1485T>G	ENSP00000496087.1:n.*1485T>G
ENST00000647468.2:c.1651T>G MANE Select	ENSP00000496731.1:p.Phe551Val
ENST00000648111.1:c.*1339T>G	ENSP00000497275.1:n.*1339T>G
ENST00000367101.5:c.*99T>G	ENSP00000356068.1:n.*99T>G
ENST00000367104.7:c.1651T>G	ENSP00000356071.3:p.Phe551Val
ENST00000435180.5:c.376T>G	ENSP00000391168.1:p.Phe126Val
ENST00000606965.5:c.*212T>G	ENSP00000475808.1:n.*212T>G
ENST00000607071.5:c.*1585T>G	ENSP00000475855.1:n.*1585T>G
ENST00000607742.5:c.*2929T>G	ENSP00000475523.1:n.*2929T>G
NM_032861.3:c.1651T>G	NP_116250.3:p.Phe551Val
NR_073096.1:n.1584T>G
XM_006715586.1:c.1441T>G	XP_006715649.1:p.Phe481Val
XM_011536196.1:c.1630T>G	XP_011534498.1:p.Phe544Val
XM_011536197.1:c.1537T>G	XP_011534499.1:p.Phe513Val
XM_011536198.1:c.1441T>G	XP_011534500.1:p.Phe481Val
XM_006715586.3:c.1441T>G	XP_006715649.1:p.Phe481Val
XM_011536196.3:c.1630T>G	XP_011534498.1:p.Phe544Val
XM_011536198.3:c.1441T>G	XP_011534500.1:p.Phe481Val
XM_024446573.1:c.1651T>G	XP_024302341.1:p.Phe551Val
XR_001743697.2:n.1682T>G
XR_942606.2:n.1733T>G
NM_032861.4:c.1651T>G MANE Select	NP_116250.3:p.Phe551Val
NR_073096.2:n.1566T>G