Canonical Allele Identifier: CA5153176

Gene: ANKS6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98751123del , CM000671.2:g.98751123del	GRCh38
NC_000009.11:g.101513405del , CM000671.1:g.101513405del	GRCh37
NC_000009.10:g.100553226del	NCBI36
NG_042237.1:g.50428del

Transcript Alleles

HGVS	Amino-acid Change
NM_173551.5:c.2327-19del MANE Select	NP_775822.3:n.2327-19del
ENST00000353234.5:c.2327-19del MANE Select	ENSP00000297837.6:n.2327-19del
NM_173551.3:c.2327-19del	NP_775822.3:n.2327-19del
NM_173551.4:c.2327-19del	NP_775822.3:n.2327-19del
ENST00000353234.4:c.2327-19del	ENSP00000297837.6:n.2327-19del
ENST00000375019.6:c.1424-19del	ENSP00000364159.2:n.1424-19del
ENST00000444472.5:c.735-19del
ENST00000634393.1:n.1427-19del
XM_005251793.3:c.2330-19del	XP_005251850.1:n.2330-19del
XM_005251793.4:c.2330-19del	XP_005251850.1:n.2330-19del
XM_005251794.3:c.2327-19del	XP_005251851.1:n.2327-19del
XM_005251794.4:c.2327-19del	XP_005251851.1:n.2327-19del
XM_006716998.2:c.2330-19del	XP_006717061.1:n.2330-19del
XM_006716998.3:c.2330-19del	XP_006717061.1:n.2330-19del
XM_006716999.2:c.2156-19del	XP_006717062.1:n.2156-19del
XM_006716999.3:c.2156-19del	XP_006717062.1:n.2156-19del
XM_011518356.1:c.2330-19del	XP_011516658.1:n.2330-19del
XM_011518357.1:c.1340-19del	XP_011516659.1:n.1340-19del
XM_017014445.1:c.2327-19del	XP_016869934.1:n.2327-19del
XM_017014447.1:c.1079-19del	XP_016869936.1:n.1079-19del
XM_024447445.1:c.2048-19del	XP_024303213.1:n.2048-19del
XM_024447447.1:c.1745-19del	XP_024303215.1:n.1745-19del
XR_001746230.1:n.1432-19del
XR_242576.3:n.2365-19del
XR_428520.2:n.2369-19del
XR_428520.3:n.2368-19del
XR_929736.1:n.2369-19del
XR_929736.2:n.2368-19del
XR_929737.1:n.1432-19del