Canonical Allele Identifier: CA366255261

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535987C>G (hg19) ; chr6:g.158114955C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114955C>G , CM000668.2:g.158114955C>G	GRCh38
NC_000006.11:g.158535987C>G , CM000668.1:g.158535987C>G	GRCh37
NC_000006.10:g.158455975C>G	NCBI36
NG_032889.1:g.58326G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.730G>C	ENSP00000391168.2:n.730G>C
ENST00000607071.6:c.*1238G>C	ENSP00000475855.1:n.*1238G>C
ENST00000642244.1:c.1428G>C	ENSP00000493554.1:p.Lys476Asn
ENST00000642903.1:c.1518G>C	ENSP00000493559.1:p.Lys506Asn
ENST00000644972.1:c.1518G>C	ENSP00000496451.1:p.Lys506Asn
ENST00000645077.1:c.*1139G>C	ENSP00000496113.1:n.*1139G>C
ENST00000645172.1:c.*1220G>C	ENSP00000495367.1:n.*1220G>C
ENST00000646190.1:n.2849G>C
ENST00000646208.1:c.1254G>C	ENSP00000493723.1:p.Lys418Asn
ENST00000646410.1:c.1389G>C	ENSP00000494205.1:p.Lys463Asn
ENST00000646562.1:c.*1352G>C	ENSP00000496087.1:n.*1352G>C
ENST00000647468.2:c.1518G>C MANE Select	ENSP00000496731.1:p.Lys506Asn
ENST00000648111.1:c.*1206G>C	ENSP00000497275.1:n.*1206G>C
ENST00000367101.5:c.1562G>C	ENSP00000356068.1:p.Arg521Thr
ENST00000367104.7:c.1518G>C	ENSP00000356071.3:p.Lys506Asn
ENST00000435180.5:c.243G>C	ENSP00000391168.1:p.Lys81Asn
ENST00000606965.5:c.*79G>C	ENSP00000475808.1:n.*79G>C
ENST00000607071.5:c.*1452G>C	ENSP00000475855.1:n.*1452G>C
ENST00000607742.5:c.*2796G>C	ENSP00000475523.1:n.*2796G>C
NM_032861.3:c.1518G>C	NP_116250.3:p.Lys506Asn
NR_073096.1:n.1451G>C
XM_006715586.1:c.1308G>C	XP_006715649.1:p.Lys436Asn
XM_011536196.1:c.1497G>C	XP_011534498.1:p.Lys499Asn
XM_011536197.1:c.1404G>C	XP_011534499.1:p.Lys468Asn
XM_011536198.1:c.1308G>C	XP_011534500.1:p.Lys436Asn
XM_006715586.3:c.1308G>C	XP_006715649.1:p.Lys436Asn
XM_011536196.3:c.1497G>C	XP_011534498.1:p.Lys499Asn
XM_011536198.3:c.1308G>C	XP_011534500.1:p.Lys436Asn
XM_024446573.1:c.1518G>C	XP_024302341.1:p.Lys506Asn
XR_001743697.2:n.1549G>C
XR_942606.2:n.1600G>C
NM_032861.4:c.1518G>C MANE Select	NP_116250.3:p.Lys506Asn
NR_073096.2:n.1433G>C