Canonical Allele Identifier: CA5153845

Gene: ANKS6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98790520G>T , CM000671.2:g.98790520G>T	GRCh38
NC_000009.11:g.101552802G>T , CM000671.1:g.101552802G>T	GRCh37
NC_000009.10:g.100592623G>T	NCBI36
NG_042237.1:g.11023C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353234.5:c.446C>A MANE Select	ENSP00000297837.6:p.Thr149Asn
ENST00000353234.4:c.446C>A	ENSP00000297837.6:p.Thr149Asn
ENST00000375019.6:c.-41-5644C>A	ENSP00000364159.2:n.-41-5644C>A
ENST00000471846.1:n.494C>A
ENST00000634393.1:n.7+5470C>A
NM_173551.3:c.446C>A	NP_775822.3:p.Thr149Asn
NM_173551.4:c.446C>A	NP_775822.3:p.Thr149Asn
XM_005251793.3:c.446C>A	XP_005251850.1:p.Thr149Asn
XM_005251794.3:c.446C>A	XP_005251851.1:p.Thr149Asn
XM_006716998.2:c.446C>A	XP_006717061.1:p.Thr149Asn
XM_006716999.2:c.272C>A	XP_006717062.1:p.Thr91Asn
XM_011518356.1:c.446C>A	XP_011516658.1:p.Thr149Asn
XR_242576.3:n.484C>A
XR_428520.2:n.485C>A
XR_929736.1:n.485C>A
XM_005251793.4:c.446C>A	XP_005251850.1:p.Thr149Asn
XM_005251794.4:c.446C>A	XP_005251851.1:p.Thr149Asn
XM_006716998.3:c.446C>A	XP_006717061.1:p.Thr149Asn
XM_006716999.3:c.272C>A	XP_006717062.1:p.Thr91Asn
XM_017014445.1:c.446C>A	XP_016869934.1:p.Thr149Asn
XM_024447445.1:c.164C>A	XP_024303213.1:p.Thr55Asn
XM_024447447.1:c.-140C>A	XP_024303215.1:n.-140C>A
XR_428520.3:n.484C>A
XR_929736.2:n.484C>A
NM_173551.5:c.446C>A MANE Select	NP_775822.3:p.Thr149Asn