Canonical Allele Identifier: CA246336364

Gene: ANKLE2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132727031A>T , CM000674.2:g.132727031A>T	GRCh38
NC_000012.11:g.133303617A>T , CM000674.1:g.133303617A>T	GRCh37
NC_000012.10:g.131813690A>T	NCBI36
NG_034022.1:g.39858T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357997.10:c.*211T>A MANE Select	ENSP00000350686.5:n.*211T>A
ENST00000357997.9:c.*211T>A	ENSP00000350686.5:n.*211T>A
ENST00000539605.5:n.9527T>A
ENST00000542282.5:c.*211T>A	ENSP00000437807.1:n.*211T>A
NM_015114.2:c.*211T>A	NP_055929.1:n.*211T>A
XM_005266159.2:c.*211T>A	XP_005266216.1:n.*211T>A
XM_005266160.1:c.*211T>A	XP_005266217.1:n.*211T>A
XM_006719735.1:c.*393T>A	XP_006719798.1:n.*393T>A
XM_011534789.1:c.*211T>A	XP_011533091.1:n.*211T>A
XM_005266159.3:c.*211T>A	XP_005266216.1:n.*211T>A
XM_005266160.2:c.*211T>A	XP_005266217.1:n.*211T>A
XM_024448899.1:c.*211T>A	XP_024304667.1:n.*211T>A
XR_001748638.1:n.2950T>A
NM_015114.3:c.*211T>A MANE Select	NP_055929.1:n.*211T>A