Canonical Allele Identifier: CA452820077

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114817-G-A
• MyVariant Identifiers: chr6:g.158535849G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114817G>A , CM000668.2:g.158114817G>A	GRCh38
NC_000006.11:g.158535849G>A , CM000668.1:g.158535849G>A	GRCh37
NC_000006.10:g.158455837G>A	NCBI36
NG_032889.1:g.58464C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1376C>T	ENSP00000475855.1:n.*1376C>T
ENST00000642244.1:c.1566C>T	ENSP00000493554.1:p.Pro522=
ENST00000642903.1:c.1656C>T	ENSP00000493559.1:p.Pro552=
ENST00000644972.1:c.1656C>T	ENSP00000496451.1:p.Pro552=
ENST00000645077.1:c.*1277C>T	ENSP00000496113.1:n.*1277C>T
ENST00000645172.1:c.*1358C>T	ENSP00000495367.1:n.*1358C>T
ENST00000646190.1:n.2987C>T
ENST00000646208.1:c.1392C>T	ENSP00000493723.1:p.Pro464=
ENST00000646410.1:c.1527C>T	ENSP00000494205.1:p.Pro509=
ENST00000646562.1:c.*1490C>T	ENSP00000496087.1:n.*1490C>T
ENST00000647468.2:c.1656C>T MANE Select	ENSP00000496731.1:p.Pro552=
ENST00000648111.1:c.*1344C>T	ENSP00000497275.1:n.*1344C>T
ENST00000367101.5:c.*104C>T	ENSP00000356068.1:n.*104C>T
ENST00000367104.7:c.1656C>T	ENSP00000356071.3:p.Pro552=
ENST00000435180.5:c.381C>T	ENSP00000391168.1:p.Pro127=
ENST00000606965.5:c.*217C>T	ENSP00000475808.1:n.*217C>T
ENST00000607071.5:c.*1590C>T	ENSP00000475855.1:n.*1590C>T
ENST00000607742.5:c.*2934C>T	ENSP00000475523.1:n.*2934C>T
NM_032861.3:c.1656C>T	NP_116250.3:p.Pro552=
NR_073096.1:n.1589C>T
XM_006715586.1:c.1446C>T	XP_006715649.1:p.Pro482=
XM_011536196.1:c.1635C>T	XP_011534498.1:p.Pro545=
XM_011536197.1:c.1542C>T	XP_011534499.1:p.Pro514=
XM_011536198.1:c.1446C>T	XP_011534500.1:p.Pro482=
XM_006715586.3:c.1446C>T	XP_006715649.1:p.Pro482=
XM_011536196.3:c.1635C>T	XP_011534498.1:p.Pro545=
XM_011536198.3:c.1446C>T	XP_011534500.1:p.Pro482=
XM_024446573.1:c.1656C>T	XP_024302341.1:p.Pro552=
XR_001743697.2:n.1687C>T
XR_942606.2:n.1738C>T
NM_032861.4:c.1656C>T MANE Select	NP_116250.3:p.Pro552=
NR_073096.2:n.1571C>T