Canonical Allele Identifier: CA366254884

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535823T>C (hg19) ; chr6:g.158114791T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114791T>C , CM000668.2:g.158114791T>C	GRCh38
NC_000006.11:g.158535823T>C , CM000668.1:g.158535823T>C	GRCh37
NC_000006.10:g.158455811T>C	NCBI36
NG_032889.1:g.58490A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000607071.6:c.*1402A>G	ENSP00000475855.1:n.*1402A>G
ENST00000642244.1:c.1592A>G	ENSP00000493554.1:p.Lys531Arg
ENST00000642903.1:c.1682A>G	ENSP00000493559.1:p.Lys561Arg
ENST00000644972.1:c.1682A>G	ENSP00000496451.1:p.Lys561Arg
ENST00000645077.1:c.*1303A>G	ENSP00000496113.1:n.*1303A>G
ENST00000645172.1:c.*1384A>G	ENSP00000495367.1:n.*1384A>G
ENST00000646190.1:n.3013A>G
ENST00000646208.1:c.1418A>G	ENSP00000493723.1:p.Lys473Arg
ENST00000646410.1:c.1553A>G	ENSP00000494205.1:p.Lys518Arg
ENST00000646562.1:c.*1516A>G	ENSP00000496087.1:n.*1516A>G
ENST00000647468.2:c.1682A>G MANE Select	ENSP00000496731.1:p.Lys561Arg
ENST00000648111.1:c.*1370A>G	ENSP00000497275.1:n.*1370A>G
ENST00000367101.5:c.*130A>G	ENSP00000356068.1:n.*130A>G
ENST00000367104.7:c.1682A>G	ENSP00000356071.3:p.Lys561Arg
ENST00000435180.5:c.407A>G	ENSP00000391168.1:p.Lys136Arg
ENST00000606965.5:c.*243A>G	ENSP00000475808.1:n.*243A>G
ENST00000607071.5:c.*1616A>G	ENSP00000475855.1:n.*1616A>G
ENST00000607742.5:c.*2960A>G	ENSP00000475523.1:n.*2960A>G
NM_032861.3:c.1682A>G	NP_116250.3:p.Lys561Arg
NR_073096.1:n.1615A>G
XM_006715586.1:c.1472A>G	XP_006715649.1:p.Lys491Arg
XM_011536196.1:c.1661A>G	XP_011534498.1:p.Lys554Arg
XM_011536197.1:c.1568A>G	XP_011534499.1:p.Lys523Arg
XM_011536198.1:c.1472A>G	XP_011534500.1:p.Lys491Arg
XM_006715586.3:c.1472A>G	XP_006715649.1:p.Lys491Arg
XM_011536196.3:c.1661A>G	XP_011534498.1:p.Lys554Arg
XM_011536198.3:c.1472A>G	XP_011534500.1:p.Lys491Arg
XM_024446573.1:c.1682A>G	XP_024302341.1:p.Lys561Arg
XR_001743697.2:n.1713A>G
XR_942606.2:n.1764A>G
NM_032861.4:c.1682A>G MANE Select	NP_116250.3:p.Lys561Arg
NR_073096.2:n.1597A>G