Canonical Allele Identifier: CA452820163

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535924T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114892T>A , CM000668.2:g.158114892T>A	GRCh38
NC_000006.11:g.158535924T>A , CM000668.1:g.158535924T>A	GRCh37
NC_000006.10:g.158455912T>A	NCBI36
NG_032889.1:g.58389A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.793A>T	ENSP00000391168.2:n.793A>T
ENST00000607071.6:c.*1301A>T	ENSP00000475855.1:n.*1301A>T
ENST00000642244.1:c.1491A>T	ENSP00000493554.1:p.Ile497=
ENST00000642903.1:c.1581A>T	ENSP00000493559.1:p.Ile527=
ENST00000644972.1:c.1581A>T	ENSP00000496451.1:p.Ile527=
ENST00000645077.1:c.*1202A>T	ENSP00000496113.1:n.*1202A>T
ENST00000645172.1:c.*1283A>T	ENSP00000495367.1:n.*1283A>T
ENST00000646190.1:n.2912A>T
ENST00000646208.1:c.1317A>T	ENSP00000493723.1:p.Ile439=
ENST00000646410.1:c.1452A>T	ENSP00000494205.1:p.Ile484=
ENST00000646562.1:c.*1415A>T	ENSP00000496087.1:n.*1415A>T
ENST00000647468.2:c.1581A>T MANE Select	ENSP00000496731.1:p.Ile527=
ENST00000648111.1:c.*1269A>T	ENSP00000497275.1:n.*1269A>T
ENST00000367101.5:c.*29A>T	ENSP00000356068.1:n.*29A>T
ENST00000367104.7:c.1581A>T	ENSP00000356071.3:p.Ile527=
ENST00000435180.5:c.306A>T	ENSP00000391168.1:p.Ile102=
ENST00000606965.5:c.*142A>T	ENSP00000475808.1:n.*142A>T
ENST00000607071.5:c.*1515A>T	ENSP00000475855.1:n.*1515A>T
ENST00000607742.5:c.*2859A>T	ENSP00000475523.1:n.*2859A>T
NM_032861.3:c.1581A>T	NP_116250.3:p.Ile527=
NR_073096.1:n.1514A>T
XM_006715586.1:c.1371A>T	XP_006715649.1:p.Ile457=
XM_011536196.1:c.1560A>T	XP_011534498.1:p.Ile520=
XM_011536197.1:c.1467A>T	XP_011534499.1:p.Ile489=
XM_011536198.1:c.1371A>T	XP_011534500.1:p.Ile457=
XM_006715586.3:c.1371A>T	XP_006715649.1:p.Ile457=
XM_011536196.3:c.1560A>T	XP_011534498.1:p.Ile520=
XM_011536198.3:c.1371A>T	XP_011534500.1:p.Ile457=
XM_024446573.1:c.1581A>T	XP_024302341.1:p.Ile527=
XR_001743697.2:n.1612A>T
XR_942606.2:n.1663A>T
NM_032861.4:c.1581A>T MANE Select	NP_116250.3:p.Ile527=
NR_073096.2:n.1496A>T