Canonical Allele Identifier: CA366255170

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535954C>G (hg19) ; chr6:g.158114922C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114922C>G , CM000668.2:g.158114922C>G	GRCh38
NC_000006.11:g.158535954C>G , CM000668.1:g.158535954C>G	GRCh37
NC_000006.10:g.158455942C>G	NCBI36
NG_032889.1:g.58359G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.763G>C	ENSP00000391168.2:n.763G>C
ENST00000607071.6:c.*1271G>C	ENSP00000475855.1:n.*1271G>C
ENST00000642244.1:c.1461G>C	ENSP00000493554.1:p.Met487Ile
ENST00000642903.1:c.1551G>C	ENSP00000493559.1:p.Met517Ile
ENST00000644972.1:c.1551G>C	ENSP00000496451.1:p.Met517Ile
ENST00000645077.1:c.*1172G>C	ENSP00000496113.1:n.*1172G>C
ENST00000645172.1:c.*1253G>C	ENSP00000495367.1:n.*1253G>C
ENST00000646190.1:n.2882G>C
ENST00000646208.1:c.1287G>C	ENSP00000493723.1:p.Met429Ile
ENST00000646410.1:c.1422G>C	ENSP00000494205.1:p.Met474Ile
ENST00000646562.1:c.*1385G>C	ENSP00000496087.1:n.*1385G>C
ENST00000647468.2:c.1551G>C MANE Select	ENSP00000496731.1:p.Met517Ile
ENST00000648111.1:c.*1239G>C	ENSP00000497275.1:n.*1239G>C
ENST00000367101.5:c.1595G>C	ENSP00000356068.1:p.Ter532Ser
ENST00000367104.7:c.1551G>C	ENSP00000356071.3:p.Met517Ile
ENST00000435180.5:c.276G>C	ENSP00000391168.1:p.Met92Ile
ENST00000606965.5:c.*112G>C	ENSP00000475808.1:n.*112G>C
ENST00000607071.5:c.*1485G>C	ENSP00000475855.1:n.*1485G>C
ENST00000607742.5:c.*2829G>C	ENSP00000475523.1:n.*2829G>C
NM_032861.3:c.1551G>C	NP_116250.3:p.Met517Ile
NR_073096.1:n.1484G>C
XM_006715586.1:c.1341G>C	XP_006715649.1:p.Met447Ile
XM_011536196.1:c.1530G>C	XP_011534498.1:p.Met510Ile
XM_011536197.1:c.1437G>C	XP_011534499.1:p.Met479Ile
XM_011536198.1:c.1341G>C	XP_011534500.1:p.Met447Ile
XM_006715586.3:c.1341G>C	XP_006715649.1:p.Met447Ile
XM_011536196.3:c.1530G>C	XP_011534498.1:p.Met510Ile
XM_011536198.3:c.1341G>C	XP_011534500.1:p.Met447Ile
XM_024446573.1:c.1551G>C	XP_024302341.1:p.Met517Ile
XR_001743697.2:n.1582G>C
XR_942606.2:n.1633G>C
NM_032861.4:c.1551G>C MANE Select	NP_116250.3:p.Met517Ile
NR_073096.2:n.1466G>C