Canonical Allele Identifier: CA431606771

Gene: SERPINE2

Linked Data

• MyVariant Identifiers: chr2:g.224862854T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223998137T>G , CM000664.2:g.223998137T>G	GRCh38
NC_000002.11:g.224862854T>G , CM000664.1:g.224862854T>G	GRCh37
NC_000002.10:g.224571098T>G	NCBI36
NG_032907.1:g.46183A>C
NG_032907.2:g.46183A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000258405.9:c.465A>C	ENSP00000258405.4:p.Ala155=
ENST00000409304.6:c.465A>C MANE Select	ENSP00000386412.1:p.Ala155=
ENST00000258405.8:c.465A>C	ENSP00000258405.4:p.Ala155=
ENST00000409304.5:c.465A>C	ENSP00000386412.1:p.Ala155=
ENST00000409840.7:c.465A>C	ENSP00000386969.3:p.Ala155=
ENST00000432738.5:c.465A>C	ENSP00000408452.1:p.Ala155=
ENST00000447280.6:c.501A>C	ENSP00000415786.2:p.Ala167=
NM_001136528.1:c.465A>C	NP_001130000.1:p.Ala155=
NM_001136530.1:c.501A>C	NP_001130002.1:p.Ala167=
NM_006216.3:c.465A>C	NP_006207.1:p.Ala155=
NR_073116.1:n.1126A>C
XM_005246641.2:c.501A>C	XP_005246698.1:p.Ala167=
XM_005246642.2:c.465A>C	XP_005246699.1:p.Ala155=
XM_017004330.1:c.465A>C	XP_016859819.1:p.Ala155=
XM_017004332.2:c.465A>C	XP_016859821.1:p.Ala155=
NM_001136528.2:c.465A>C MANE Select	NP_001130000.1:p.Ala155=
NM_006216.4:c.465A>C	NP_006207.1:p.Ala155=
NR_073116.2:n.1126A>C