Canonical Allele Identifier: CA366254987

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535871T>A (hg19) ; chr6:g.158114839T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114839T>A , CM000668.2:g.158114839T>A	GRCh38
NC_000006.11:g.158535871T>A , CM000668.1:g.158535871T>A	GRCh37
NC_000006.10:g.158455859T>A	NCBI36
NG_032889.1:g.58442A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.846A>T	ENSP00000391168.2:n.846A>T
ENST00000607071.6:c.*1354A>T	ENSP00000475855.1:n.*1354A>T
ENST00000642244.1:c.1544A>T	ENSP00000493554.1:p.Asn515Ile
ENST00000642903.1:c.1634A>T	ENSP00000493559.1:p.Asn545Ile
ENST00000644972.1:c.1634A>T	ENSP00000496451.1:p.Asn545Ile
ENST00000645077.1:c.*1255A>T	ENSP00000496113.1:n.*1255A>T
ENST00000645172.1:c.*1336A>T	ENSP00000495367.1:n.*1336A>T
ENST00000646190.1:n.2965A>T
ENST00000646208.1:c.1370A>T	ENSP00000493723.1:p.Asn457Ile
ENST00000646410.1:c.1505A>T	ENSP00000494205.1:p.Asn502Ile
ENST00000646562.1:c.*1468A>T	ENSP00000496087.1:n.*1468A>T
ENST00000647468.2:c.1634A>T MANE Select	ENSP00000496731.1:p.Asn545Ile
ENST00000648111.1:c.*1322A>T	ENSP00000497275.1:n.*1322A>T
ENST00000367101.5:c.*82A>T	ENSP00000356068.1:n.*82A>T
ENST00000367104.7:c.1634A>T	ENSP00000356071.3:p.Asn545Ile
ENST00000435180.5:c.359A>T	ENSP00000391168.1:p.Asn120Ile
ENST00000606965.5:c.*195A>T	ENSP00000475808.1:n.*195A>T
ENST00000607071.5:c.*1568A>T	ENSP00000475855.1:n.*1568A>T
ENST00000607742.5:c.*2912A>T	ENSP00000475523.1:n.*2912A>T
NM_032861.3:c.1634A>T	NP_116250.3:p.Asn545Ile
NR_073096.1:n.1567A>T
XM_006715586.1:c.1424A>T	XP_006715649.1:p.Asn475Ile
XM_011536196.1:c.1613A>T	XP_011534498.1:p.Asn538Ile
XM_011536197.1:c.1520A>T	XP_011534499.1:p.Asn507Ile
XM_011536198.1:c.1424A>T	XP_011534500.1:p.Asn475Ile
XM_006715586.3:c.1424A>T	XP_006715649.1:p.Asn475Ile
XM_011536196.3:c.1613A>T	XP_011534498.1:p.Asn538Ile
XM_011536198.3:c.1424A>T	XP_011534500.1:p.Asn475Ile
XM_024446573.1:c.1634A>T	XP_024302341.1:p.Asn545Ile
XR_001743697.2:n.1665A>T
XR_942606.2:n.1716A>T
NM_032861.4:c.1634A>T MANE Select	NP_116250.3:p.Asn545Ile
NR_073096.2:n.1549A>T