Canonical Allele Identifier: CA387403894

Gene: ANKLE2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132727400G>A , CM000674.2:g.132727400G>A	GRCh38
NC_000012.11:g.133303986G>A , CM000674.1:g.133303986G>A	GRCh37
NC_000012.10:g.131814059G>A	NCBI36
NG_034022.1:g.39489C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015114.3:c.2659C>T MANE Select	NP_055929.1:p.Pro887Ser
ENST00000357997.10:c.2659C>T MANE Select	ENSP00000350686.5:p.Pro887Ser
NM_015114.2:c.2659C>T	NP_055929.1:p.Pro887Ser
ENST00000357997.9:c.2659C>T	ENSP00000350686.5:p.Pro887Ser
ENST00000538766.1:c.724C>T	ENSP00000445760.1:p.Pro242Ser
ENST00000539605.5:n.9158C>T
ENST00000542282.5:c.724C>T	ENSP00000437807.1:p.Pro242Ser
ENST00000542374.5:n.401C>T
ENST00000542657.5:c.724C>T	ENSP00000438551.1:p.Pro242Ser
XM_005266159.2:c.2473C>T	XP_005266216.1:p.Pro825Ser
XM_005266159.3:c.2473C>T	XP_005266216.1:p.Pro825Ser
XM_005266160.1:c.2473C>T	XP_005266217.1:p.Pro825Ser
XM_005266160.2:c.2473C>T	XP_005266217.1:p.Pro825Ser
XM_006719735.1:c.*24C>T	XP_006719798.1:n.*24C>T
XM_011534789.1:c.1348C>T	XP_011533091.1:p.Pro450Ser
XM_024448899.1:c.1348C>T	XP_024304667.1:p.Pro450Ser
XR_001748638.1:n.2581C>T