Canonical Allele Identifier: CA5153588

Gene: ANKS6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98782446C>A , CM000671.2:g.98782446C>A	GRCh38
NC_000009.11:g.101544728C>A , CM000671.1:g.101544728C>A	GRCh37
NC_000009.10:g.100584549C>A	NCBI36
NG_042237.1:g.19097G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_173551.5:c.1219+21G>T MANE Select	NP_775822.3:n.1219+21G>T
ENST00000353234.5:c.1219+21G>T MANE Select	ENSP00000297837.6:n.1219+21G>T
NM_173551.3:c.1219+21G>T	NP_775822.3:n.1219+21G>T
NM_173551.4:c.1219+21G>T	NP_775822.3:n.1219+21G>T
ENST00000353234.4:c.1219+21G>T	ENSP00000297837.6:n.1219+21G>T
ENST00000375019.6:c.316+21G>T	ENSP00000364159.2:n.316+21G>T
ENST00000634393.1:n.319+21G>T
XM_005251793.3:c.1219+21G>T	XP_005251850.1:n.1219+21G>T
XM_005251793.4:c.1219+21G>T	XP_005251850.1:n.1219+21G>T
XM_005251794.3:c.1219+21G>T	XP_005251851.1:n.1219+21G>T
XM_005251794.4:c.1219+21G>T	XP_005251851.1:n.1219+21G>T
XM_006716998.2:c.1219+21G>T	XP_006717061.1:n.1219+21G>T
XM_006716998.3:c.1219+21G>T	XP_006717061.1:n.1219+21G>T
XM_006716999.2:c.1045+21G>T	XP_006717062.1:n.1045+21G>T
XM_006716999.3:c.1045+21G>T	XP_006717062.1:n.1045+21G>T
XM_011518356.1:c.1219+21G>T	XP_011516658.1:n.1219+21G>T
XM_011518357.1:c.229+21G>T	XP_011516659.1:n.229+21G>T
XM_017014445.1:c.1219+21G>T	XP_016869934.1:n.1219+21G>T
XM_017014447.1:c.9+21G>T	XP_016869936.1:n.9+21G>T
XM_024447445.1:c.937+21G>T	XP_024303213.1:n.937+21G>T
XM_024447447.1:c.634+21G>T	XP_024303215.1:n.634+21G>T
XR_001746230.1:n.324+21G>T
XR_242576.3:n.1257+21G>T
XR_428520.2:n.1258+21G>T
XR_428520.3:n.1257+21G>T
XR_929736.1:n.1258+21G>T
XR_929736.2:n.1257+21G>T
XR_929737.1:n.324+21G>T