Canonical Allele Identifier: CA11139050
Gene: SERPINE2 HGNC NCBI

Linked Data

dbSNP Id: rs7579646

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224035979G>A , CM000664.2:g.224035979G>A GRCh38
NC_000002.11:g.224900696G>A , CM000664.1:g.224900696G>A GRCh37
NC_000002.10:g.224608940G>A NCBI36
NG_032907.1:g.8341C>T
NG_032907.2:g.8341C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258405.9:c.-23+3120C>T ENSP00000258405.4:n.-23+3120C>T
ENST00000409304.6:c.-23+3120C>T MANE Select ENSP00000386412.1:n.-23+3120C>T
ENST00000258405.8:c.-23+3120C>T ENSP00000258405.4:n.-23+3120C>T
ENST00000409304.5:c.-23+3120C>T ENSP00000386412.1:n.-23+3120C>T
ENST00000447280.6:c.14+2511C>T ENSP00000415786.2:n.14+2511C>T
ENST00000454956.1:c.-67+3120C>T ENSP00000399655.1:n.-67+3120C>T
ENST00000489065.1:n.192+3120C>T
NM_001136528.1:c.-23+3120C>T NP_001130000.1:n.-23+3120C>T
NM_001136530.1:c.14+2511C>T NP_001130002.1:n.14+2511C>T
NM_006216.3:c.-23+3120C>T NP_006207.1:n.-23+3120C>T
XM_005246641.2:c.14+2511C>T XP_005246698.1:n.14+2511C>T
NM_001136528.2:c.-23+3120C>T MANE Select NP_001130000.1:n.-23+3120C>T
NM_006216.4:c.-23+3120C>T NP_006207.1:n.-23+3120C>T