Canonical Allele Identifier: CA351124588

Gene: SERPINE2

Linked Data

• dbSNP Id: rs11548971
• COSMIC: COSM6157308 ; COSM6157309
• MyVariant Identifiers: chr2:g.224862913A>G (hg19) ; chr2:g.223998196A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223998196A>G , CM000664.2:g.223998196A>G	GRCh38
NC_000002.11:g.224862913A>G , CM000664.1:g.224862913A>G	GRCh37
NC_000002.10:g.224571157A>G	NCBI36
NG_032907.1:g.46124T>C
NG_032907.2:g.46124T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258405.9:c.406T>C	ENSP00000258405.4:p.Cys136Arg
ENST00000409304.6:c.406T>C MANE Select	ENSP00000386412.1:p.Cys136Arg
ENST00000258405.8:c.406T>C	ENSP00000258405.4:p.Cys136Arg
ENST00000409304.5:c.406T>C	ENSP00000386412.1:p.Cys136Arg
ENST00000409840.7:c.406T>C	ENSP00000386969.3:p.Cys136Arg
ENST00000432738.5:c.406T>C	ENSP00000408452.1:p.Cys136Arg
ENST00000447280.6:c.442T>C	ENSP00000415786.2:p.Cys148Arg
NM_001136528.1:c.406T>C	NP_001130000.1:p.Cys136Arg
NM_001136530.1:c.442T>C	NP_001130002.1:p.Cys148Arg
NM_006216.3:c.406T>C	NP_006207.1:p.Cys136Arg
NR_073116.1:n.1067T>C
XM_005246641.2:c.442T>C	XP_005246698.1:p.Cys148Arg
XM_005246642.2:c.406T>C	XP_005246699.1:p.Cys136Arg
XM_017004330.1:c.406T>C	XP_016859819.1:p.Cys136Arg
XM_017004332.2:c.406T>C	XP_016859821.1:p.Cys136Arg
NM_001136528.2:c.406T>C MANE Select	NP_001130000.1:p.Cys136Arg
NM_006216.4:c.406T>C	NP_006207.1:p.Cys136Arg
NR_073116.2:n.1067T>C