Canonical Allele Identifier: CA5153788

Gene: ANKS6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98790302G>A , CM000671.2:g.98790302G>A	GRCh38
NC_000009.11:g.101552584G>A , CM000671.1:g.101552584G>A	GRCh37
NC_000009.10:g.100592405G>A	NCBI36
NG_042237.1:g.11241C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353234.5:c.664C>T MANE Select	ENSP00000297837.6:p.Arg222Trp
ENST00000353234.4:c.664C>T	ENSP00000297837.6:p.Arg222Trp
ENST00000375019.6:c.-41-5426C>T	ENSP00000364159.2:n.-41-5426C>T
ENST00000466120.1:n.195C>T
ENST00000471846.1:n.712C>T
ENST00000634393.1:n.7+5688C>T
NM_173551.3:c.664C>T	NP_775822.3:p.Arg222Trp
NM_173551.4:c.664C>T	NP_775822.3:p.Arg222Trp
XM_005251793.3:c.664C>T	XP_005251850.1:p.Arg222Trp
XM_005251794.3:c.664C>T	XP_005251851.1:p.Arg222Trp
XM_006716998.2:c.664C>T	XP_006717061.1:p.Arg222Trp
XM_006716999.2:c.490C>T	XP_006717062.1:p.Arg164Trp
XM_011518356.1:c.664C>T	XP_011516658.1:p.Arg222Trp
XR_242576.3:n.702C>T
XR_428520.2:n.703C>T
XR_929736.1:n.703C>T
XM_005251793.4:c.664C>T	XP_005251850.1:p.Arg222Trp
XM_005251794.4:c.664C>T	XP_005251851.1:p.Arg222Trp
XM_006716998.3:c.664C>T	XP_006717061.1:p.Arg222Trp
XM_006716999.3:c.490C>T	XP_006717062.1:p.Arg164Trp
XM_017014445.1:c.664C>T	XP_016869934.1:p.Arg222Trp
XM_024447445.1:c.382C>T	XP_024303213.1:p.Arg128Trp
XM_024447447.1:c.79C>T	XP_024303215.1:p.Arg27Trp
XR_428520.3:n.702C>T
XR_929736.2:n.702C>T
NM_173551.5:c.664C>T MANE Select	NP_775822.3:p.Arg222Trp