Canonical Allele Identifier: CA366254985

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535870A>C (hg19) ; chr6:g.158114838A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114838A>C , CM000668.2:g.158114838A>C	GRCh38
NC_000006.11:g.158535870A>C , CM000668.1:g.158535870A>C	GRCh37
NC_000006.10:g.158455858A>C	NCBI36
NG_032889.1:g.58443T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.847T>G	ENSP00000391168.2:n.847T>G
ENST00000607071.6:c.*1355T>G	ENSP00000475855.1:n.*1355T>G
ENST00000642244.1:c.1545T>G	ENSP00000493554.1:p.Asn515Lys
ENST00000642903.1:c.1635T>G	ENSP00000493559.1:p.Asn545Lys
ENST00000644972.1:c.1635T>G	ENSP00000496451.1:p.Asn545Lys
ENST00000645077.1:c.*1256T>G	ENSP00000496113.1:n.*1256T>G
ENST00000645172.1:c.*1337T>G	ENSP00000495367.1:n.*1337T>G
ENST00000646190.1:n.2966T>G
ENST00000646208.1:c.1371T>G	ENSP00000493723.1:p.Asn457Lys
ENST00000646410.1:c.1506T>G	ENSP00000494205.1:p.Asn502Lys
ENST00000646562.1:c.*1469T>G	ENSP00000496087.1:n.*1469T>G
ENST00000647468.2:c.1635T>G MANE Select	ENSP00000496731.1:p.Asn545Lys
ENST00000648111.1:c.*1323T>G	ENSP00000497275.1:n.*1323T>G
ENST00000367101.5:c.*83T>G	ENSP00000356068.1:n.*83T>G
ENST00000367104.7:c.1635T>G	ENSP00000356071.3:p.Asn545Lys
ENST00000435180.5:c.360T>G	ENSP00000391168.1:p.Asn120Lys
ENST00000606965.5:c.*196T>G	ENSP00000475808.1:n.*196T>G
ENST00000607071.5:c.*1569T>G	ENSP00000475855.1:n.*1569T>G
ENST00000607742.5:c.*2913T>G	ENSP00000475523.1:n.*2913T>G
NM_032861.3:c.1635T>G	NP_116250.3:p.Asn545Lys
NR_073096.1:n.1568T>G
XM_006715586.1:c.1425T>G	XP_006715649.1:p.Asn475Lys
XM_011536196.1:c.1614T>G	XP_011534498.1:p.Asn538Lys
XM_011536197.1:c.1521T>G	XP_011534499.1:p.Asn507Lys
XM_011536198.1:c.1425T>G	XP_011534500.1:p.Asn475Lys
XM_006715586.3:c.1425T>G	XP_006715649.1:p.Asn475Lys
XM_011536196.3:c.1614T>G	XP_011534498.1:p.Asn538Lys
XM_011536198.3:c.1425T>G	XP_011534500.1:p.Asn475Lys
XM_024446573.1:c.1635T>G	XP_024302341.1:p.Asn545Lys
XR_001743697.2:n.1666T>G
XR_942606.2:n.1717T>G
NM_032861.4:c.1635T>G MANE Select	NP_116250.3:p.Asn545Lys
NR_073096.2:n.1550T>G