Canonical Allele Identifier: CA6895317

Gene: ANKLE2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132730026C>T , CM000674.2:g.132730026C>T	GRCh38
NC_000012.11:g.133306612C>T , CM000674.1:g.133306612C>T	GRCh37
NC_000012.10:g.131816685C>T	NCBI36
NG_034022.1:g.36863G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015114.3:c.2136G>A MANE Select	NP_055929.1:p.Ala712=
ENST00000357997.10:c.2136G>A MANE Select	ENSP00000350686.5:p.Ala712=
NM_015114.2:c.2136G>A	NP_055929.1:p.Ala712=
ENST00000357997.9:c.2136G>A	ENSP00000350686.5:p.Ala712=
ENST00000505031.6:n.2558G>A
ENST00000538766.1:c.201G>A	ENSP00000445760.1:p.Ala67=
ENST00000539605.5:n.8635G>A
ENST00000542282.5:c.201G>A	ENSP00000437807.1:p.Ala67=
ENST00000542374.5:n.226-1863G>A
ENST00000542657.5:c.201G>A	ENSP00000438551.1:p.Ala67=
XM_005266159.2:c.1950G>A	XP_005266216.1:p.Ala650=
XM_005266159.3:c.1950G>A	XP_005266216.1:p.Ala650=
XM_005266160.1:c.1950G>A	XP_005266217.1:p.Ala650=
XM_005266160.2:c.1950G>A	XP_005266217.1:p.Ala650=
XM_006719735.1:c.1892-1863G>A	XP_006719798.1:n.1892-1863G>A
XM_011534789.1:c.825G>A	XP_011533091.1:p.Ala275=
XM_024448899.1:c.825G>A	XP_024304667.1:p.Ala275=
XR_001748638.1:n.2058G>A