Canonical Allele Identifier: CA366255173

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535955A>G (hg19) ; chr6:g.158114923A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114923A>G , CM000668.2:g.158114923A>G	GRCh38
NC_000006.11:g.158535955A>G , CM000668.1:g.158535955A>G	GRCh37
NC_000006.10:g.158455943A>G	NCBI36
NG_032889.1:g.58358T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.762T>C	ENSP00000391168.2:n.762T>C
ENST00000607071.6:c.*1270T>C	ENSP00000475855.1:n.*1270T>C
ENST00000642244.1:c.1460T>C	ENSP00000493554.1:p.Met487Thr
ENST00000642903.1:c.1550T>C	ENSP00000493559.1:p.Met517Thr
ENST00000644972.1:c.1550T>C	ENSP00000496451.1:p.Met517Thr
ENST00000645077.1:c.*1171T>C	ENSP00000496113.1:n.*1171T>C
ENST00000645172.1:c.*1252T>C	ENSP00000495367.1:n.*1252T>C
ENST00000646190.1:n.2881T>C
ENST00000646208.1:c.1286T>C	ENSP00000493723.1:p.Met429Thr
ENST00000646410.1:c.1421T>C	ENSP00000494205.1:p.Met474Thr
ENST00000646562.1:c.*1384T>C	ENSP00000496087.1:n.*1384T>C
ENST00000647468.2:c.1550T>C MANE Select	ENSP00000496731.1:p.Met517Thr
ENST00000648111.1:c.*1238T>C	ENSP00000497275.1:n.*1238T>C
ENST00000367101.5:c.1594T>C	ENSP00000356068.1:p.Ter532Arg
ENST00000367104.7:c.1550T>C	ENSP00000356071.3:p.Met517Thr
ENST00000435180.5:c.275T>C	ENSP00000391168.1:p.Met92Thr
ENST00000606965.5:c.*111T>C	ENSP00000475808.1:n.*111T>C
ENST00000607071.5:c.*1484T>C	ENSP00000475855.1:n.*1484T>C
ENST00000607742.5:c.*2828T>C	ENSP00000475523.1:n.*2828T>C
NM_032861.3:c.1550T>C	NP_116250.3:p.Met517Thr
NR_073096.1:n.1483T>C
XM_006715586.1:c.1340T>C	XP_006715649.1:p.Met447Thr
XM_011536196.1:c.1529T>C	XP_011534498.1:p.Met510Thr
XM_011536197.1:c.1436T>C	XP_011534499.1:p.Met479Thr
XM_011536198.1:c.1340T>C	XP_011534500.1:p.Met447Thr
XM_006715586.3:c.1340T>C	XP_006715649.1:p.Met447Thr
XM_011536196.3:c.1529T>C	XP_011534498.1:p.Met510Thr
XM_011536198.3:c.1340T>C	XP_011534500.1:p.Met447Thr
XM_024446573.1:c.1550T>C	XP_024302341.1:p.Met517Thr
XR_001743697.2:n.1581T>C
XR_942606.2:n.1632T>C
NM_032861.4:c.1550T>C MANE Select	NP_116250.3:p.Met517Thr
NR_073096.2:n.1465T>C