Canonical Allele Identifier: CA2396537813

Gene: SERPIND1 PI4KA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20779813_20779814delinsAG , CM000684.2:g.20779813_20779814delinsAG	GRCh38
NC_000022.10:g.21134101_21134102delinsAG , CM000684.1:g.21134101_21134102delinsAG	GRCh37
NC_000022.9:g.19464101_19464102delinsAG	NCBI36
NG_012076.1:g.10719_10720delinsAG
NG_033052.1:g.83999_84000delinsCT
NG_012076.2:g.10719_10720delinsAG
NG_033052.2:g.83999_84000delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215727.10:c.501_502delinsAG (SERPIND1) MANE Select	ENSP00000215727.5:p.Leu167=
ENST00000255882.11:c.2328+13379_2328+13380delinsCT (PI4KA) MANE Select	ENSP00000255882.6:n.2328+13379_2328+13380delinsCT
ENST00000215727.9:c.501_502delinsAG (SERPIND1)	ENSP00000215727.5:p.Leu167=
ENST00000255882.10:c.2328+13379_2328+13380delinsCT (PI4KA)	ENSP00000255882.6:n.2328+13379_2328+13380delinsCT
ENST00000406799.1:c.501_502delinsAG (SERPIND1)	ENSP00000384050.1:p.Leu167=
ENST00000466162.5:n.91+13379_91+13380delinsCT (PI4KA)
ENST00000484220.1:n.64+13379_64+13380delinsCT (PI4KA)
NM_000185.3:c.501_502delinsAG (SERPIND1)	NP_000176.2:p.Leu167=
NM_058004.3:c.2328+13379_2328+13380delinsCT (PI4KA)	NP_477352.3:n.2328+13379_2328+13380delinsCT
XM_005261634.1:c.2412+13379_2412+13380delinsCT (PI4KA)	XP_005261691.1:n.2412+13379_2412+13380delinsCT
XM_005261635.1:c.2412+13379_2412+13380delinsCT (PI4KA)	XP_005261692.1:n.2412+13379_2412+13380delinsCT
XM_011530226.1:c.2412+13379_2412+13380delinsCT (PI4KA)	XP_011528528.1:n.2412+13379_2412+13380delinsCT
XM_011530227.1:c.2412+13379_2412+13380delinsCT (PI4KA)	XP_011528529.1:n.2412+13379_2412+13380delinsCT
XM_011530228.1:c.2412+13379_2412+13380delinsCT (PI4KA)	XP_011528530.1:n.2412+13379_2412+13380delinsCT
XR_937868.1:n.2415+13379_2415+13380delinsCT (PI4KA)
NM_001362862.1:c.2328+13379_2328+13380delinsCT (PI4KA)	NP_001349791.1:n.2328+13379_2328+13380delinsCT
NM_001362863.1:c.2262+13379_2262+13380delinsCT (PI4KA)	NP_001349792.1:n.2262+13379_2262+13380delinsCT
XM_011530228.2:c.2412+13379_2412+13380delinsCT (PI4KA)	XP_011528530.1:n.2412+13379_2412+13380delinsCT
XM_017028830.1:c.429+13379_429+13380delinsCT (PI4KA)	XP_016884319.1:n.429+13379_429+13380delinsCT
XR_001755251.1:n.2415+13379_2415+13380delinsCT (PI4KA)
NM_000185.4:c.501_502delinsAG (SERPIND1) MANE Select	NP_000176.2:p.Leu167=
NM_058004.4:c.2328+13379_2328+13380delinsCT (PI4KA) MANE Select	NP_477352.3:n.2328+13379_2328+13380delinsCT
NM_001362862.2:c.2328+13379_2328+13380delinsCT (PI4KA)	NP_001349791.1:n.2328+13379_2328+13380delinsCT
NM_001362863.2:c.2262+13379_2262+13380delinsCT (PI4KA)	NP_001349792.1:n.2262+13379_2262+13380delinsCT