Canonical Allele Identifier: CA452820069

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535837G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114805G>A , CM000668.2:g.158114805G>A	GRCh38
NC_000006.11:g.158535837G>A , CM000668.1:g.158535837G>A	GRCh37
NC_000006.10:g.158455825G>A	NCBI36
NG_032889.1:g.58476C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1388C>T	ENSP00000475855.1:n.*1388C>T
ENST00000642244.1:c.1578C>T	ENSP00000493554.1:p.Val526=
ENST00000642903.1:c.1668C>T	ENSP00000493559.1:p.Val556=
ENST00000644972.1:c.1668C>T	ENSP00000496451.1:p.Val556=
ENST00000645077.1:c.*1289C>T	ENSP00000496113.1:n.*1289C>T
ENST00000645172.1:c.*1370C>T	ENSP00000495367.1:n.*1370C>T
ENST00000646190.1:n.2999C>T
ENST00000646208.1:c.1404C>T	ENSP00000493723.1:p.Val468=
ENST00000646410.1:c.1539C>T	ENSP00000494205.1:p.Val513=
ENST00000646562.1:c.*1502C>T	ENSP00000496087.1:n.*1502C>T
ENST00000647468.2:c.1668C>T MANE Select	ENSP00000496731.1:p.Val556=
ENST00000648111.1:c.*1356C>T	ENSP00000497275.1:n.*1356C>T
ENST00000367101.5:c.*116C>T	ENSP00000356068.1:n.*116C>T
ENST00000367104.7:c.1668C>T	ENSP00000356071.3:p.Val556=
ENST00000435180.5:c.393C>T	ENSP00000391168.1:p.Val131=
ENST00000606965.5:c.*229C>T	ENSP00000475808.1:n.*229C>T
ENST00000607071.5:c.*1602C>T	ENSP00000475855.1:n.*1602C>T
ENST00000607742.5:c.*2946C>T	ENSP00000475523.1:n.*2946C>T
NM_032861.3:c.1668C>T	NP_116250.3:p.Val556=
NR_073096.1:n.1601C>T
XM_006715586.1:c.1458C>T	XP_006715649.1:p.Val486=
XM_011536196.1:c.1647C>T	XP_011534498.1:p.Val549=
XM_011536197.1:c.1554C>T	XP_011534499.1:p.Val518=
XM_011536198.1:c.1458C>T	XP_011534500.1:p.Val486=
XM_006715586.3:c.1458C>T	XP_006715649.1:p.Val486=
XM_011536196.3:c.1647C>T	XP_011534498.1:p.Val549=
XM_011536198.3:c.1458C>T	XP_011534500.1:p.Val486=
XM_024446573.1:c.1668C>T	XP_024302341.1:p.Val556=
XR_001743697.2:n.1699C>T
XR_942606.2:n.1750C>T
NM_032861.4:c.1668C>T MANE Select	NP_116250.3:p.Val556=
NR_073096.2:n.1583C>T