Canonical Allele Identifier: CA366255045

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535899C>G (hg19) ; chr6:g.158114867C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114867C>G , CM000668.2:g.158114867C>G	GRCh38
NC_000006.11:g.158535899C>G , CM000668.1:g.158535899C>G	GRCh37
NC_000006.10:g.158455887C>G	NCBI36
NG_032889.1:g.58414G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.818G>C	ENSP00000391168.2:n.818G>C
ENST00000607071.6:c.*1326G>C	ENSP00000475855.1:n.*1326G>C
ENST00000642244.1:c.1516G>C	ENSP00000493554.1:p.Gly506Arg
ENST00000642903.1:c.1606G>C	ENSP00000493559.1:p.Gly536Arg
ENST00000644972.1:c.1606G>C	ENSP00000496451.1:p.Gly536Arg
ENST00000645077.1:c.*1227G>C	ENSP00000496113.1:n.*1227G>C
ENST00000645172.1:c.*1308G>C	ENSP00000495367.1:n.*1308G>C
ENST00000646190.1:n.2937G>C
ENST00000646208.1:c.1342G>C	ENSP00000493723.1:p.Gly448Arg
ENST00000646410.1:c.1477G>C	ENSP00000494205.1:p.Gly493Arg
ENST00000646562.1:c.*1440G>C	ENSP00000496087.1:n.*1440G>C
ENST00000647468.2:c.1606G>C MANE Select	ENSP00000496731.1:p.Gly536Arg
ENST00000648111.1:c.*1294G>C	ENSP00000497275.1:n.*1294G>C
ENST00000367101.5:c.*54G>C	ENSP00000356068.1:n.*54G>C
ENST00000367104.7:c.1606G>C	ENSP00000356071.3:p.Gly536Arg
ENST00000435180.5:c.331G>C	ENSP00000391168.1:p.Gly111Arg
ENST00000606965.5:c.*167G>C	ENSP00000475808.1:n.*167G>C
ENST00000607071.5:c.*1540G>C	ENSP00000475855.1:n.*1540G>C
ENST00000607742.5:c.*2884G>C	ENSP00000475523.1:n.*2884G>C
NM_032861.3:c.1606G>C	NP_116250.3:p.Gly536Arg
NR_073096.1:n.1539G>C
XM_006715586.1:c.1396G>C	XP_006715649.1:p.Gly466Arg
XM_011536196.1:c.1585G>C	XP_011534498.1:p.Gly529Arg
XM_011536197.1:c.1492G>C	XP_011534499.1:p.Gly498Arg
XM_011536198.1:c.1396G>C	XP_011534500.1:p.Gly466Arg
XM_006715586.3:c.1396G>C	XP_006715649.1:p.Gly466Arg
XM_011536196.3:c.1585G>C	XP_011534498.1:p.Gly529Arg
XM_011536198.3:c.1396G>C	XP_011534500.1:p.Gly466Arg
XM_024446573.1:c.1606G>C	XP_024302341.1:p.Gly536Arg
XR_001743697.2:n.1637G>C
XR_942606.2:n.1688G>C
NM_032861.4:c.1606G>C MANE Select	NP_116250.3:p.Gly536Arg
NR_073096.2:n.1521G>C