Canonical Allele Identifier: CA366255076

Gene: SERAC1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.804G>C	ENSP00000391168.2:n.804G>C
ENST00000607071.6:c.*1312G>C	ENSP00000475855.1:n.*1312G>C
ENST00000642244.1:c.1502G>C	ENSP00000493554.1:p.Ser501Thr
ENST00000642903.1:c.1592G>C	ENSP00000493559.1:p.Ser531Thr
ENST00000644972.1:c.1592G>C	ENSP00000496451.1:p.Ser531Thr
ENST00000645077.1:c.*1213G>C	ENSP00000496113.1:n.*1213G>C
ENST00000645172.1:c.*1294G>C	ENSP00000495367.1:n.*1294G>C
ENST00000646190.1:n.2923G>C
ENST00000646208.1:c.1328G>C	ENSP00000493723.1:p.Ser443Thr
ENST00000646410.1:c.1463G>C	ENSP00000494205.1:p.Ser488Thr
ENST00000646562.1:c.*1426G>C	ENSP00000496087.1:n.*1426G>C
ENST00000647468.2:c.1592G>C MANE Select	ENSP00000496731.1:p.Ser531Thr
ENST00000648111.1:c.*1280G>C	ENSP00000497275.1:n.*1280G>C
ENST00000367101.5:c.*40G>C	ENSP00000356068.1:n.*40G>C
ENST00000367104.7:c.1592G>C	ENSP00000356071.3:p.Ser531Thr
ENST00000435180.5:c.317G>C	ENSP00000391168.1:p.Ser106Thr
ENST00000606965.5:c.*153G>C	ENSP00000475808.1:n.*153G>C
ENST00000607071.5:c.*1526G>C	ENSP00000475855.1:n.*1526G>C
ENST00000607742.5:c.*2870G>C	ENSP00000475523.1:n.*2870G>C
NM_032861.3:c.1592G>C	NP_116250.3:p.Ser531Thr
NR_073096.1:n.1525G>C
XM_006715586.1:c.1382G>C	XP_006715649.1:p.Ser461Thr
XM_011536196.1:c.1571G>C	XP_011534498.1:p.Ser524Thr
XM_011536197.1:c.1478G>C	XP_011534499.1:p.Ser493Thr
XM_011536198.1:c.1382G>C	XP_011534500.1:p.Ser461Thr
XM_006715586.3:c.1382G>C	XP_006715649.1:p.Ser461Thr
XM_011536196.3:c.1571G>C	XP_011534498.1:p.Ser524Thr
XM_011536198.3:c.1382G>C	XP_011534500.1:p.Ser461Thr
XM_024446573.1:c.1592G>C	XP_024302341.1:p.Ser531Thr
XR_001743697.2:n.1623G>C
XR_942606.2:n.1674G>C
NM_032861.4:c.1592G>C MANE Select	NP_116250.3:p.Ser531Thr
NR_073096.2:n.1507G>C