Canonical Allele Identifier: CA452820062

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535822C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114790C>T , CM000668.2:g.158114790C>T	GRCh38
NC_000006.11:g.158535822C>T , CM000668.1:g.158535822C>T	GRCh37
NC_000006.10:g.158455810C>T	NCBI36
NG_032889.1:g.58491G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000607071.6:c.*1403G>A	ENSP00000475855.1:n.*1403G>A
ENST00000642244.1:c.1593G>A	ENSP00000493554.1:p.Lys531=
ENST00000642903.1:c.1683G>A	ENSP00000493559.1:p.Lys561=
ENST00000644972.1:c.1683G>A	ENSP00000496451.1:p.Lys561=
ENST00000645077.1:c.*1304G>A	ENSP00000496113.1:n.*1304G>A
ENST00000645172.1:c.*1385G>A	ENSP00000495367.1:n.*1385G>A
ENST00000646190.1:n.3014G>A
ENST00000646208.1:c.1419G>A	ENSP00000493723.1:p.Lys473=
ENST00000646410.1:c.1554G>A	ENSP00000494205.1:p.Lys518=
ENST00000646562.1:c.*1517G>A	ENSP00000496087.1:n.*1517G>A
ENST00000647468.2:c.1683G>A MANE Select	ENSP00000496731.1:p.Lys561=
ENST00000648111.1:c.*1371G>A	ENSP00000497275.1:n.*1371G>A
ENST00000367101.5:c.*131G>A	ENSP00000356068.1:n.*131G>A
ENST00000367104.7:c.1683G>A	ENSP00000356071.3:p.Lys561=
ENST00000435180.5:c.408G>A	ENSP00000391168.1:p.Lys136=
ENST00000606965.5:c.*244G>A	ENSP00000475808.1:n.*244G>A
ENST00000607071.5:c.*1617G>A	ENSP00000475855.1:n.*1617G>A
ENST00000607742.5:c.*2961G>A	ENSP00000475523.1:n.*2961G>A
NM_032861.3:c.1683G>A	NP_116250.3:p.Lys561=
NR_073096.1:n.1616G>A
XM_006715586.1:c.1473G>A	XP_006715649.1:p.Lys491=
XM_011536196.1:c.1662G>A	XP_011534498.1:p.Lys554=
XM_011536197.1:c.1569G>A	XP_011534499.1:p.Lys523=
XM_011536198.1:c.1473G>A	XP_011534500.1:p.Lys491=
XM_006715586.3:c.1473G>A	XP_006715649.1:p.Lys491=
XM_011536196.3:c.1662G>A	XP_011534498.1:p.Lys554=
XM_011536198.3:c.1473G>A	XP_011534500.1:p.Lys491=
XM_024446573.1:c.1683G>A	XP_024302341.1:p.Lys561=
XR_001743697.2:n.1714G>A
XR_942606.2:n.1765G>A
NM_032861.4:c.1683G>A MANE Select	NP_116250.3:p.Lys561=
NR_073096.2:n.1598G>A