Canonical Allele Identifier: CA366255092

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535920A>C (hg19) ; chr6:g.158114888A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114888A>C , CM000668.2:g.158114888A>C	GRCh38
NC_000006.11:g.158535920A>C , CM000668.1:g.158535920A>C	GRCh37
NC_000006.10:g.158455908A>C	NCBI36
NG_032889.1:g.58393T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.797T>G	ENSP00000391168.2:n.797T>G
ENST00000607071.6:c.*1305T>G	ENSP00000475855.1:n.*1305T>G
ENST00000642244.1:c.1495T>G	ENSP00000493554.1:p.Phe499Val
ENST00000642903.1:c.1585T>G	ENSP00000493559.1:p.Phe529Val
ENST00000644972.1:c.1585T>G	ENSP00000496451.1:p.Phe529Val
ENST00000645077.1:c.*1206T>G	ENSP00000496113.1:n.*1206T>G
ENST00000645172.1:c.*1287T>G	ENSP00000495367.1:n.*1287T>G
ENST00000646190.1:n.2916T>G
ENST00000646208.1:c.1321T>G	ENSP00000493723.1:p.Phe441Val
ENST00000646410.1:c.1456T>G	ENSP00000494205.1:p.Phe486Val
ENST00000646562.1:c.*1419T>G	ENSP00000496087.1:n.*1419T>G
ENST00000647468.2:c.1585T>G MANE Select	ENSP00000496731.1:p.Phe529Val
ENST00000648111.1:c.*1273T>G	ENSP00000497275.1:n.*1273T>G
ENST00000367101.5:c.*33T>G	ENSP00000356068.1:n.*33T>G
ENST00000367104.7:c.1585T>G	ENSP00000356071.3:p.Phe529Val
ENST00000435180.5:c.310T>G	ENSP00000391168.1:p.Phe104Val
ENST00000606965.5:c.*146T>G	ENSP00000475808.1:n.*146T>G
ENST00000607071.5:c.*1519T>G	ENSP00000475855.1:n.*1519T>G
ENST00000607742.5:c.*2863T>G	ENSP00000475523.1:n.*2863T>G
NM_032861.3:c.1585T>G	NP_116250.3:p.Phe529Val
NR_073096.1:n.1518T>G
XM_006715586.1:c.1375T>G	XP_006715649.1:p.Phe459Val
XM_011536196.1:c.1564T>G	XP_011534498.1:p.Phe522Val
XM_011536197.1:c.1471T>G	XP_011534499.1:p.Phe491Val
XM_011536198.1:c.1375T>G	XP_011534500.1:p.Phe459Val
XM_006715586.3:c.1375T>G	XP_006715649.1:p.Phe459Val
XM_011536196.3:c.1564T>G	XP_011534498.1:p.Phe522Val
XM_011536198.3:c.1375T>G	XP_011534500.1:p.Phe459Val
XM_024446573.1:c.1585T>G	XP_024302341.1:p.Phe529Val
XR_001743697.2:n.1616T>G
XR_942606.2:n.1667T>G
NM_032861.4:c.1585T>G MANE Select	NP_116250.3:p.Phe529Val
NR_073096.2:n.1500T>G