Canonical Allele Identifier: CA366254997

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535875C>T (hg19) ; chr6:g.158114843C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114843C>T , CM000668.2:g.158114843C>T	GRCh38
NC_000006.11:g.158535875C>T , CM000668.1:g.158535875C>T	GRCh37
NC_000006.10:g.158455863C>T	NCBI36
NG_032889.1:g.58438G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.842G>A	ENSP00000391168.2:n.842G>A
ENST00000607071.6:c.*1350G>A	ENSP00000475855.1:n.*1350G>A
ENST00000642244.1:c.1540G>A	ENSP00000493554.1:p.Val514Ile
ENST00000642903.1:c.1630G>A	ENSP00000493559.1:p.Val544Ile
ENST00000644972.1:c.1630G>A	ENSP00000496451.1:p.Val544Ile
ENST00000645077.1:c.*1251G>A	ENSP00000496113.1:n.*1251G>A
ENST00000645172.1:c.*1332G>A	ENSP00000495367.1:n.*1332G>A
ENST00000646190.1:n.2961G>A
ENST00000646208.1:c.1366G>A	ENSP00000493723.1:p.Val456Ile
ENST00000646410.1:c.1501G>A	ENSP00000494205.1:p.Val501Ile
ENST00000646562.1:c.*1464G>A	ENSP00000496087.1:n.*1464G>A
ENST00000647468.2:c.1630G>A MANE Select	ENSP00000496731.1:p.Val544Ile
ENST00000648111.1:c.*1318G>A	ENSP00000497275.1:n.*1318G>A
ENST00000367101.5:c.*78G>A	ENSP00000356068.1:n.*78G>A
ENST00000367104.7:c.1630G>A	ENSP00000356071.3:p.Val544Ile
ENST00000435180.5:c.355G>A	ENSP00000391168.1:p.Val119Ile
ENST00000606965.5:c.*191G>A	ENSP00000475808.1:n.*191G>A
ENST00000607071.5:c.*1564G>A	ENSP00000475855.1:n.*1564G>A
ENST00000607742.5:c.*2908G>A	ENSP00000475523.1:n.*2908G>A
NM_032861.3:c.1630G>A	NP_116250.3:p.Val544Ile
NR_073096.1:n.1563G>A
XM_006715586.1:c.1420G>A	XP_006715649.1:p.Val474Ile
XM_011536196.1:c.1609G>A	XP_011534498.1:p.Val537Ile
XM_011536197.1:c.1516G>A	XP_011534499.1:p.Val506Ile
XM_011536198.1:c.1420G>A	XP_011534500.1:p.Val474Ile
XM_006715586.3:c.1420G>A	XP_006715649.1:p.Val474Ile
XM_011536196.3:c.1609G>A	XP_011534498.1:p.Val537Ile
XM_011536198.3:c.1420G>A	XP_011534500.1:p.Val474Ile
XM_024446573.1:c.1630G>A	XP_024302341.1:p.Val544Ile
XR_001743697.2:n.1661G>A
XR_942606.2:n.1712G>A
NM_032861.4:c.1630G>A MANE Select	NP_116250.3:p.Val544Ile
NR_073096.2:n.1545G>A