Canonical Allele Identifier: CA366255075

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535913C>A (hg19) ; chr6:g.158114881C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114881C>A , CM000668.2:g.158114881C>A	GRCh38
NC_000006.11:g.158535913C>A , CM000668.1:g.158535913C>A	GRCh37
NC_000006.10:g.158455901C>A	NCBI36
NG_032889.1:g.58400G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.804G>T	ENSP00000391168.2:n.804G>T
ENST00000607071.6:c.*1312G>T	ENSP00000475855.1:n.*1312G>T
ENST00000642244.1:c.1502G>T	ENSP00000493554.1:p.Ser501Ile
ENST00000642903.1:c.1592G>T	ENSP00000493559.1:p.Ser531Ile
ENST00000644972.1:c.1592G>T	ENSP00000496451.1:p.Ser531Ile
ENST00000645077.1:c.*1213G>T	ENSP00000496113.1:n.*1213G>T
ENST00000645172.1:c.*1294G>T	ENSP00000495367.1:n.*1294G>T
ENST00000646190.1:n.2923G>T
ENST00000646208.1:c.1328G>T	ENSP00000493723.1:p.Ser443Ile
ENST00000646410.1:c.1463G>T	ENSP00000494205.1:p.Ser488Ile
ENST00000646562.1:c.*1426G>T	ENSP00000496087.1:n.*1426G>T
ENST00000647468.2:c.1592G>T MANE Select	ENSP00000496731.1:p.Ser531Ile
ENST00000648111.1:c.*1280G>T	ENSP00000497275.1:n.*1280G>T
ENST00000367101.5:c.*40G>T	ENSP00000356068.1:n.*40G>T
ENST00000367104.7:c.1592G>T	ENSP00000356071.3:p.Ser531Ile
ENST00000435180.5:c.317G>T	ENSP00000391168.1:p.Ser106Ile
ENST00000606965.5:c.*153G>T	ENSP00000475808.1:n.*153G>T
ENST00000607071.5:c.*1526G>T	ENSP00000475855.1:n.*1526G>T
ENST00000607742.5:c.*2870G>T	ENSP00000475523.1:n.*2870G>T
NM_032861.3:c.1592G>T	NP_116250.3:p.Ser531Ile
NR_073096.1:n.1525G>T
XM_006715586.1:c.1382G>T	XP_006715649.1:p.Ser461Ile
XM_011536196.1:c.1571G>T	XP_011534498.1:p.Ser524Ile
XM_011536197.1:c.1478G>T	XP_011534499.1:p.Ser493Ile
XM_011536198.1:c.1382G>T	XP_011534500.1:p.Ser461Ile
XM_006715586.3:c.1382G>T	XP_006715649.1:p.Ser461Ile
XM_011536196.3:c.1571G>T	XP_011534498.1:p.Ser524Ile
XM_011536198.3:c.1382G>T	XP_011534500.1:p.Ser461Ile
XM_024446573.1:c.1592G>T	XP_024302341.1:p.Ser531Ile
XR_001743697.2:n.1623G>T
XR_942606.2:n.1674G>T
NM_032861.4:c.1592G>T MANE Select	NP_116250.3:p.Ser531Ile
NR_073096.2:n.1507G>T