Canonical Allele Identifier: CA6895154

Gene: ANKLE2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132728018C>T , CM000674.2:g.132728018C>T	GRCh38
NC_000012.11:g.133304604C>T , CM000674.1:g.133304604C>T	GRCh37
NC_000012.10:g.131814677C>T	NCBI36
NG_034022.1:g.38871G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357997.10:c.2615+14G>A MANE Select	ENSP00000350686.5:n.2615+14G>A
ENST00000357997.9:c.2615+14G>A	ENSP00000350686.5:n.2615+14G>A
ENST00000538766.1:c.680+14G>A	ENSP00000445760.1:n.680+14G>A
ENST00000539605.5:n.9114+14G>A
ENST00000542282.5:c.680+14G>A	ENSP00000437807.1:n.680+14G>A
ENST00000542374.5:n.357+14G>A
ENST00000542657.5:c.680+14G>A	ENSP00000438551.1:n.680+14G>A
NM_015114.2:c.2615+14G>A	NP_055929.1:n.2615+14G>A
XM_005266159.2:c.2429+14G>A	XP_005266216.1:n.2429+14G>A
XM_005266160.1:c.2429+14G>A	XP_005266217.1:n.2429+14G>A
XM_006719735.1:c.2023+14G>A	XP_006719798.1:n.2023+14G>A
XM_011534789.1:c.1304+14G>A	XP_011533091.1:n.1304+14G>A
XM_005266159.3:c.2429+14G>A	XP_005266216.1:n.2429+14G>A
XM_005266160.2:c.2429+14G>A	XP_005266217.1:n.2429+14G>A
XM_024448899.1:c.1304+14G>A	XP_024304667.1:n.1304+14G>A
XR_001748638.1:n.2537+14G>A
NM_015114.3:c.2615+14G>A MANE Select	NP_055929.1:n.2615+14G>A