Canonical Allele Identifier: CA1331343332

Gene: SERPINE2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224035127T>A , CM000664.2:g.224035127T>A	GRCh38
NC_000002.11:g.224899844T>A , CM000664.1:g.224899844T>A	GRCh37
NC_000002.10:g.224608088T>A	NCBI36
NG_032907.1:g.9193A>T
NG_032907.2:g.9193A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258405.9:c.-23+3972A>T	ENSP00000258405.4:n.-23+3972A>T
ENST00000409304.6:c.-23+3972A>T MANE Select	ENSP00000386412.1:n.-23+3972A>T
ENST00000258405.8:c.-23+3972A>T	ENSP00000258405.4:n.-23+3972A>T
ENST00000409304.5:c.-23+3972A>T	ENSP00000386412.1:n.-23+3972A>T
ENST00000447280.6:c.14+3363A>T	ENSP00000415786.2:n.14+3363A>T
ENST00000454956.1:c.-67+3972A>T	ENSP00000399655.1:n.-67+3972A>T
ENST00000489065.1:n.192+3972A>T
NM_001136528.1:c.-23+3972A>T	NP_001130000.1:n.-23+3972A>T
NM_001136530.1:c.14+3363A>T	NP_001130002.1:n.14+3363A>T
NM_006216.3:c.-23+3972A>T	NP_006207.1:n.-23+3972A>T
XM_005246641.2:c.14+3363A>T	XP_005246698.1:n.14+3363A>T
NM_001136528.2:c.-23+3972A>T MANE Select	NP_001130000.1:n.-23+3972A>T
NM_006216.4:c.-23+3972A>T	NP_006207.1:n.-23+3972A>T