Canonical Allele Identifier: CA366254998

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114845-G-C
• MyVariant Identifiers: chr6:g.158535877G>C (hg19) ; chr6:g.158114845G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114845G>C , CM000668.2:g.158114845G>C	GRCh38
NC_000006.11:g.158535877G>C , CM000668.1:g.158535877G>C	GRCh37
NC_000006.10:g.158455865G>C	NCBI36
NG_032889.1:g.58436C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.840C>G	ENSP00000391168.2:n.840C>G
ENST00000607071.6:c.*1348C>G	ENSP00000475855.1:n.*1348C>G
ENST00000642244.1:c.1538C>G	ENSP00000493554.1:p.Ser513Cys
ENST00000642903.1:c.1628C>G	ENSP00000493559.1:p.Ser543Cys
ENST00000644972.1:c.1628C>G	ENSP00000496451.1:p.Ser543Cys
ENST00000645077.1:c.*1249C>G	ENSP00000496113.1:n.*1249C>G
ENST00000645172.1:c.*1330C>G	ENSP00000495367.1:n.*1330C>G
ENST00000646190.1:n.2959C>G
ENST00000646208.1:c.1364C>G	ENSP00000493723.1:p.Ser455Cys
ENST00000646410.1:c.1499C>G	ENSP00000494205.1:p.Ser500Cys
ENST00000646562.1:c.*1462C>G	ENSP00000496087.1:n.*1462C>G
ENST00000647468.2:c.1628C>G MANE Select	ENSP00000496731.1:p.Ser543Cys
ENST00000648111.1:c.*1316C>G	ENSP00000497275.1:n.*1316C>G
ENST00000367101.5:c.*76C>G	ENSP00000356068.1:n.*76C>G
ENST00000367104.7:c.1628C>G	ENSP00000356071.3:p.Ser543Cys
ENST00000435180.5:c.353C>G	ENSP00000391168.1:p.Ser118Cys
ENST00000606965.5:c.*189C>G	ENSP00000475808.1:n.*189C>G
ENST00000607071.5:c.*1562C>G	ENSP00000475855.1:n.*1562C>G
ENST00000607742.5:c.*2906C>G	ENSP00000475523.1:n.*2906C>G
NM_032861.3:c.1628C>G	NP_116250.3:p.Ser543Cys
NR_073096.1:n.1561C>G
XM_006715586.1:c.1418C>G	XP_006715649.1:p.Ser473Cys
XM_011536196.1:c.1607C>G	XP_011534498.1:p.Ser536Cys
XM_011536197.1:c.1514C>G	XP_011534499.1:p.Ser505Cys
XM_011536198.1:c.1418C>G	XP_011534500.1:p.Ser473Cys
XM_006715586.3:c.1418C>G	XP_006715649.1:p.Ser473Cys
XM_011536196.3:c.1607C>G	XP_011534498.1:p.Ser536Cys
XM_011536198.3:c.1418C>G	XP_011534500.1:p.Ser473Cys
XM_024446573.1:c.1628C>G	XP_024302341.1:p.Ser543Cys
XR_001743697.2:n.1659C>G
XR_942606.2:n.1710C>G
NM_032861.4:c.1628C>G MANE Select	NP_116250.3:p.Ser543Cys
NR_073096.2:n.1543C>G