Canonical Allele Identifier: CA694032608

Gene: ANKS1B

Linked Data

• dbSNP Id: rs1452090048
• MyVariant Identifiers: chr12:g.99131681_99131683del (hg19) ; chr12:g.98737903_98737905del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98737904_98737906del , CM000674.2:g.98737904_98737906del	GRCh38
NC_000012.11:g.99131682_99131684del , CM000674.1:g.99131682_99131684del	GRCh37
NC_000012.10:g.97655813_97655815del	NCBI36
NG_029860.1:g.1251750_1251752del
NG_029860.2:g.1251750_1251752del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341752.11:c.691-2271_691-2269del	ENSP00000345510.6:n.691-2271_691-2269del
ENST00000547010.5:c.2221-2271_2221-2269del	ENSP00000448512.1:n.2221-2271_2221-2269del
ENST00000547776.6:c.3673-2271_3673-2269del	ENSP00000449629.2:n.3673-2271_3673-2269del
ENST00000549558.6:c.1171-2271_1171-2269del	ENSP00000448993.2:n.1171-2271_1171-2269del
ENST00000551212.1:n.317-2271_317-2269del
ENST00000555119.1:c.83-2271_83-2269del
NM_001204081.1:c.691-2271_691-2269del	NP_001191010.1:n.691-2271_691-2269del
NM_020140.3:c.1171-2271_1171-2269del	NP_064525.1:n.1171-2271_1171-2269del
NM_152788.4:c.3673-2271_3673-2269del	NP_690001.3:n.3673-2271_3673-2269del
XM_006719507.2:c.3748-2271_3748-2269del	XP_006719570.1:n.3748-2271_3748-2269del
XM_006719514.2:c.3481-2271_3481-2269del	XP_006719577.1:n.3481-2271_3481-2269del
XR_944628.1:n.4564-2271_4564-2269del
XR_944629.1:n.4564-7399_4564-7397del
NM_001352196.1:c.1423-2271_1423-2269del	NP_001339125.1:n.1423-2271_1423-2269del
NM_001352197.1:c.1351-2271_1351-2269del	NP_001339126.1:n.1351-2271_1351-2269del
NM_001352213.1:c.466-2271_466-2269del	NP_001339142.1:n.466-2271_466-2269del
NM_001352214.1:c.466-2271_466-2269del	NP_001339143.1:n.466-2271_466-2269del
NM_001352216.1:c.466-2271_466-2269del	NP_001339145.1:n.466-2271_466-2269del
NM_001352223.1:c.766-2271_766-2269del	NP_001339152.1:n.766-2271_766-2269del
XM_006719507.4:c.3748-2271_3748-2269del	XP_006719570.1:n.3748-2271_3748-2269del
XM_006719514.4:c.3481-2271_3481-2269del	XP_006719577.1:n.3481-2271_3481-2269del
XM_017019653.2:c.3745-2271_3745-2269del	XP_016875142.1:n.3745-2271_3745-2269del
XM_017019654.2:c.3733-2271_3733-2269del	XP_016875143.1:n.3733-2271_3733-2269del
XM_017019658.2:c.3493-2271_3493-2269del	XP_016875147.1:n.3493-2271_3493-2269del
XM_024449068.1:c.1324-2271_1324-2269del	XP_024304836.1:n.1324-2271_1324-2269del
XM_024449070.1:c.1255-2271_1255-2269del	XP_024304838.1:n.1255-2271_1255-2269del
NM_001204081.2:c.691-2271_691-2269del	NP_001191010.1:n.691-2271_691-2269del
NM_001352196.2:c.1423-2271_1423-2269del	NP_001339125.1:n.1423-2271_1423-2269del
NM_001352197.2:c.1351-2271_1351-2269del	NP_001339126.1:n.1351-2271_1351-2269del
NM_001352213.2:c.466-2271_466-2269del	NP_001339142.1:n.466-2271_466-2269del
NM_001352214.2:c.466-2271_466-2269del	NP_001339143.1:n.466-2271_466-2269del
NM_001352216.2:c.466-2271_466-2269del	NP_001339145.1:n.466-2271_466-2269del
NM_001352223.2:c.766-2271_766-2269del	NP_001339152.1:n.766-2271_766-2269del
NM_020140.4:c.1171-2271_1171-2269del	NP_064525.1:n.1171-2271_1171-2269del