Canonical Allele Identifier: CA366254900

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535830G>C (hg19) ; chr6:g.158114798G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114798G>C , CM000668.2:g.158114798G>C	GRCh38
NC_000006.11:g.158535830G>C , CM000668.1:g.158535830G>C	GRCh37
NC_000006.10:g.158455818G>C	NCBI36
NG_032889.1:g.58483C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1395C>G	ENSP00000475855.1:n.*1395C>G
ENST00000642244.1:c.1585C>G	ENSP00000493554.1:p.Leu529Val
ENST00000642903.1:c.1675C>G	ENSP00000493559.1:p.Leu559Val
ENST00000644972.1:c.1675C>G	ENSP00000496451.1:p.Leu559Val
ENST00000645077.1:c.*1296C>G	ENSP00000496113.1:n.*1296C>G
ENST00000645172.1:c.*1377C>G	ENSP00000495367.1:n.*1377C>G
ENST00000646190.1:n.3006C>G
ENST00000646208.1:c.1411C>G	ENSP00000493723.1:p.Leu471Val
ENST00000646410.1:c.1546C>G	ENSP00000494205.1:p.Leu516Val
ENST00000646562.1:c.*1509C>G	ENSP00000496087.1:n.*1509C>G
ENST00000647468.2:c.1675C>G MANE Select	ENSP00000496731.1:p.Leu559Val
ENST00000648111.1:c.*1363C>G	ENSP00000497275.1:n.*1363C>G
ENST00000367101.5:c.*123C>G	ENSP00000356068.1:n.*123C>G
ENST00000367104.7:c.1675C>G	ENSP00000356071.3:p.Leu559Val
ENST00000435180.5:c.400C>G	ENSP00000391168.1:p.Leu134Val
ENST00000606965.5:c.*236C>G	ENSP00000475808.1:n.*236C>G
ENST00000607071.5:c.*1609C>G	ENSP00000475855.1:n.*1609C>G
ENST00000607742.5:c.*2953C>G	ENSP00000475523.1:n.*2953C>G
NM_032861.3:c.1675C>G	NP_116250.3:p.Leu559Val
NR_073096.1:n.1608C>G
XM_006715586.1:c.1465C>G	XP_006715649.1:p.Leu489Val
XM_011536196.1:c.1654C>G	XP_011534498.1:p.Leu552Val
XM_011536197.1:c.1561C>G	XP_011534499.1:p.Leu521Val
XM_011536198.1:c.1465C>G	XP_011534500.1:p.Leu489Val
XM_006715586.3:c.1465C>G	XP_006715649.1:p.Leu489Val
XM_011536196.3:c.1654C>G	XP_011534498.1:p.Leu552Val
XM_011536198.3:c.1465C>G	XP_011534500.1:p.Leu489Val
XM_024446573.1:c.1675C>G	XP_024302341.1:p.Leu559Val
XR_001743697.2:n.1706C>G
XR_942606.2:n.1757C>G
NM_032861.4:c.1675C>G MANE Select	NP_116250.3:p.Leu559Val
NR_073096.2:n.1590C>G