Canonical Allele Identifier: CA387361750

Gene: ANKLE2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132754714C>A , CM000674.2:g.132754714C>A	GRCh38
NC_000012.11:g.133331300C>A , CM000674.1:g.133331300C>A	GRCh37
NC_000012.10:g.131841373C>A	NCBI36
NG_034022.1:g.12175G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015114.3:c.601G>T MANE Select	NP_055929.1:p.Gly201Trp
ENST00000357997.10:c.601G>T MANE Select	ENSP00000350686.5:p.Gly201Trp
NM_015114.2:c.601G>T	NP_055929.1:p.Gly201Trp
ENST00000357997.9:c.601G>T	ENSP00000350686.5:p.Gly201Trp
ENST00000539605.5:n.7100G>T
XM_005266159.2:c.415G>T	XP_005266216.1:p.Gly139Trp
XM_005266159.3:c.415G>T	XP_005266216.1:p.Gly139Trp
XM_005266160.1:c.415G>T	XP_005266217.1:p.Gly139Trp
XM_005266160.2:c.415G>T	XP_005266217.1:p.Gly139Trp
XM_005266161.1:c.601G>T	XP_005266218.1:p.Gly201Trp
XM_006719735.1:c.601G>T	XP_006719798.1:p.Gly201Trp
XM_011534787.1:c.601G>T	XP_011533089.1:p.Gly201Trp
XM_011534787.3:c.601G>T	XP_011533089.1:p.Gly201Trp
XM_011534788.1:c.601G>T	XP_011533090.1:p.Gly201Trp
XM_024448899.1:c.-794G>T	XP_024304667.1:n.-794G>T
XR_001748638.1:n.602G>T