Canonical Allele Identifier: CA5153887

Gene: ANKS6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98796327G>A , CM000671.2:g.98796327G>A	GRCh38
NC_000009.11:g.101558609G>A , CM000671.1:g.101558609G>A	GRCh37
NC_000009.10:g.100598430G>A	NCBI36
NG_042237.1:g.5216C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353234.5:c.165C>T MANE Select	ENSP00000297837.6:p.Ala55=
ENST00000353234.4:c.165C>T	ENSP00000297837.6:p.Ala55=
ENST00000375019.6:c.-42+357C>T	ENSP00000364159.2:n.-42+357C>T
ENST00000471846.1:n.213C>T
NM_173551.3:c.165C>T	NP_775822.3:p.Ala55=
NM_173551.4:c.165C>T	NP_775822.3:p.Ala55=
XM_005251793.3:c.165C>T	XP_005251850.1:p.Ala55=
XM_005251794.3:c.165C>T	XP_005251851.1:p.Ala55=
XM_006716998.2:c.165C>T	XP_006717061.1:p.Ala55=
XM_011518356.1:c.165C>T	XP_011516658.1:p.Ala55=
XR_242576.3:n.203C>T
XR_428520.2:n.204C>T
XR_929736.1:n.204C>T
XM_005251793.4:c.165C>T	XP_005251850.1:p.Ala55=
XM_005251794.4:c.165C>T	XP_005251851.1:p.Ala55=
XM_006716998.3:c.165C>T	XP_006717061.1:p.Ala55=
XM_017014445.1:c.165C>T	XP_016869934.1:p.Ala55=
XR_428520.3:n.203C>T
XR_929736.2:n.203C>T
NM_173551.5:c.165C>T MANE Select	NP_775822.3:p.Ala55=