Canonical Allele Identifier: CA452820094

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535867A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114835A>G , CM000668.2:g.158114835A>G	GRCh38
NC_000006.11:g.158535867A>G , CM000668.1:g.158535867A>G	GRCh37
NC_000006.10:g.158455855A>G	NCBI36
NG_032889.1:g.58446T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.850T>C	ENSP00000391168.2:n.850T>C
ENST00000607071.6:c.*1358T>C	ENSP00000475855.1:n.*1358T>C
ENST00000642244.1:c.1548T>C	ENSP00000493554.1:p.Ile516=
ENST00000642903.1:c.1638T>C	ENSP00000493559.1:p.Ile546=
ENST00000644972.1:c.1638T>C	ENSP00000496451.1:p.Ile546=
ENST00000645077.1:c.*1259T>C	ENSP00000496113.1:n.*1259T>C
ENST00000645172.1:c.*1340T>C	ENSP00000495367.1:n.*1340T>C
ENST00000646190.1:n.2969T>C
ENST00000646208.1:c.1374T>C	ENSP00000493723.1:p.Ile458=
ENST00000646410.1:c.1509T>C	ENSP00000494205.1:p.Ile503=
ENST00000646562.1:c.*1472T>C	ENSP00000496087.1:n.*1472T>C
ENST00000647468.2:c.1638T>C MANE Select	ENSP00000496731.1:p.Ile546=
ENST00000648111.1:c.*1326T>C	ENSP00000497275.1:n.*1326T>C
ENST00000367101.5:c.*86T>C	ENSP00000356068.1:n.*86T>C
ENST00000367104.7:c.1638T>C	ENSP00000356071.3:p.Ile546=
ENST00000435180.5:c.363T>C	ENSP00000391168.1:p.Ile121=
ENST00000606965.5:c.*199T>C	ENSP00000475808.1:n.*199T>C
ENST00000607071.5:c.*1572T>C	ENSP00000475855.1:n.*1572T>C
ENST00000607742.5:c.*2916T>C	ENSP00000475523.1:n.*2916T>C
NM_032861.3:c.1638T>C	NP_116250.3:p.Ile546=
NR_073096.1:n.1571T>C
XM_006715586.1:c.1428T>C	XP_006715649.1:p.Ile476=
XM_011536196.1:c.1617T>C	XP_011534498.1:p.Ile539=
XM_011536197.1:c.1524T>C	XP_011534499.1:p.Ile508=
XM_011536198.1:c.1428T>C	XP_011534500.1:p.Ile476=
XM_006715586.3:c.1428T>C	XP_006715649.1:p.Ile476=
XM_011536196.3:c.1617T>C	XP_011534498.1:p.Ile539=
XM_011536198.3:c.1428T>C	XP_011534500.1:p.Ile476=
XM_024446573.1:c.1638T>C	XP_024302341.1:p.Ile546=
XR_001743697.2:n.1669T>C
XR_942606.2:n.1720T>C
NM_032861.4:c.1638T>C MANE Select	NP_116250.3:p.Ile546=
NR_073096.2:n.1553T>C