Canonical Allele Identifier: CA452822504

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158571573C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158150541C>A , CM000668.2:g.158150541C>A	GRCh38
NC_000006.11:g.158571573C>A , CM000668.1:g.158571573C>A	GRCh37
NC_000006.10:g.158491561C>A	NCBI36
NG_032889.1:g.22740G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*11G>T	ENSP00000475855.1:n.*11G>T
ENST00000642244.1:c.177G>T	ENSP00000493554.1:p.Val59=
ENST00000642903.1:c.177G>T	ENSP00000493559.1:p.Val59=
ENST00000643093.1:n.227G>T
ENST00000644972.1:c.177G>T	ENSP00000496451.1:p.Val59=
ENST00000645077.1:c.*11G>T	ENSP00000496113.1:n.*11G>T
ENST00000645172.1:c.*11G>T	ENSP00000495367.1:n.*11G>T
ENST00000646190.1:n.1408G>T
ENST00000646208.1:c.92-3628G>T	ENSP00000493723.1:n.92-3628G>T
ENST00000646410.1:c.138G>T	ENSP00000494205.1:p.Val46=
ENST00000646562.1:c.*11G>T	ENSP00000496087.1:n.*11G>T
ENST00000647468.2:c.177G>T MANE Select	ENSP00000496731.1:p.Val59=
ENST00000648111.1:c.151G>T	ENSP00000497275.1:p.Asp51Tyr
ENST00000367101.5:c.177G>T	ENSP00000356068.1:p.Val59=
ENST00000367104.7:c.177G>T	ENSP00000356071.3:p.Val59=
ENST00000606965.5:c.177G>T	ENSP00000475808.1:p.Val59=
ENST00000607000.1:c.177G>T	ENSP00000475788.1:p.Val59=
ENST00000607071.5:c.*11G>T	ENSP00000475855.1:n.*11G>T
ENST00000607742.5:c.*11G>T	ENSP00000475523.1:n.*11G>T
NM_032861.3:c.177G>T	NP_116250.3:p.Val59=
NR_073096.1:n.319G>T
XM_006715586.1:c.-34G>T	XP_006715649.1:n.-34G>T
XM_011536196.1:c.156G>T	XP_011534498.1:p.Val52=
XM_011536197.1:c.177G>T	XP_011534499.1:p.Val59=
XM_011536198.1:c.-34G>T	XP_011534500.1:n.-34G>T
XR_942606.1:n.178G>T
XM_006715586.3:c.-34G>T	XP_006715649.1:n.-34G>T
XM_011536196.3:c.156G>T	XP_011534498.1:p.Val52=
XM_011536198.3:c.-34G>T	XP_011534500.1:n.-34G>T
XM_024446573.1:c.177G>T	XP_024302341.1:p.Val59=
XR_001743697.2:n.258G>T
XR_942606.2:n.309G>T
NM_032861.4:c.177G>T MANE Select	NP_116250.3:p.Val59=
NR_073096.2:n.301G>T