Canonical Allele Identifier: CA891800163

Gene: AXDND1

Linked Data

• dbSNP Id: rs1180005063
• MyVariant Identifiers: chr1:g.179469212del (hg19) ; chr1:g.179500077del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179500079del , CM000663.2:g.179500079del	GRCh38
NC_000001.10:g.179469214del , CM000663.1:g.179469214del	GRCh37
NC_000001.9:g.177735837del	NCBI36
NG_033075.1:g.139360del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367618.8:c.2388+7128del MANE Select	ENSP00000356590.3:n.2388+7128del
ENST00000367618.7:c.2388+7128del	ENSP00000356590.3:n.2388+7128del
ENST00000434088.1:c.2190+7128del	ENSP00000391716.1:n.2190+7128del
ENST00000457238.6:c.*367+7128del	ENSP00000416712.3:n.*367+7128del
ENST00000484883.1:n.132+7128del
ENST00000511157.5:c.*564-6754del	ENSP00000424373.1:n.*564-6754del
ENST00000617277.4:c.*563+7128del	ENSP00000482167.1:n.*563+7128del
NM_144696.5:c.2388+7128del	NP_653297.3:n.2388+7128del
NR_073544.1:n.2415-6754del
XM_011509165.1:c.2388+7128del	XP_011507467.1:n.2388+7128del
XM_011509166.1:c.2388+7128del	XP_011507468.1:n.2388+7128del
XM_011509167.1:c.2388+7128del	XP_011507469.1:n.2388+7128del
XM_011509168.1:c.2388+7128del	XP_011507470.1:n.2388+7128del
XM_011509169.1:c.2325+7128del	XP_011507471.1:n.2325+7128del
XM_011509170.1:c.2388+7128del	XP_011507472.1:n.2388+7128del
XM_011509171.1:c.2262+7128del	XP_011507473.1:n.2262+7128del
XM_011509172.1:c.2262+7128del	XP_011507474.1:n.2262+7128del
XM_011509173.1:c.2262+7128del	XP_011507475.1:n.2262+7128del
XM_011509174.1:c.2388+7128del	XP_011507476.1:n.2388+7128del
XM_011509175.1:c.2388+7128del	XP_011507477.1:n.2388+7128del
XM_011509176.1:c.2092-9217del	XP_011507478.1:n.2092-9217del
XM_011509177.1:c.2388+7128del	XP_011507479.1:n.2388+7128del
XM_011509179.1:c.1752+7128del	XP_011507481.1:n.1752+7128del
XM_011509180.1:c.2389-6754del	XP_011507482.1:n.2389-6754del
XM_011509181.1:c.1311+7128del	XP_011507483.1:n.1311+7128del
XR_921741.1:n.2755-4713del
XR_921742.1:n.2755-4713del
XM_011509166.3:c.2388+7128del	XP_011507468.1:n.2388+7128del
XM_011509167.3:c.2388+7128del	XP_011507469.1:n.2388+7128del
XM_011509179.2:c.1752+7128del	XP_011507481.1:n.1752+7128del
XM_011509181.2:c.1311+7128del	XP_011507483.1:n.1311+7128del
XM_017000257.2:c.1647+7128del	XP_016855746.1:n.1647+7128del
XM_017000258.2:c.1509+7128del	XP_016855747.1:n.1509+7128del
XM_024453104.1:c.2262+7128del	XP_024308872.1:n.2262+7128del
XM_024453107.1:c.2262+7128del	XP_024308875.1:n.2262+7128del
XR_921742.2:n.2755-4713del
NM_144696.6:c.2388+7128del MANE Select	NP_653297.3:n.2388+7128del
NR_073544.2:n.2343-6754del