Canonical Allele Identifier: CA1188354890

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110064547_110064548delinsTA , CM000663.2:g.110064547_110064548delinsTA GRCh38
NC_000001.10:g.110607169_110607170delinsTA , CM000663.1:g.110607169_110607170delinsTA GRCh37
NC_000001.9:g.110408692_110408693delinsTA NCBI36
NG_012039.1:g.11153_11154delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647563.2:c.594+39_594+40delinsTA (ALX3) MANE Select ENSP00000497310.1:n.594+39_594+40delinsTA
ENST00000649954.1:c.165+39_165+40delinsTA (ALX3) ENSP00000497035.1:n.165+39_165+40delinsTA
ENST00000369792.4:c.594+39_594+40delinsTA (ALX3) ENSP00000358807.3:n.594+39_594+40delinsTA
ENST00000473429.5:n.4214-7908_4214-7907delinsTA (STRIP1)
NM_006492.2:c.594+39_594+40delinsTA (ALX3) NP_006483.2:n.594+39_594+40delinsTA
NM_006492.3:c.594+39_594+40delinsTA (ALX3) MANE Select NP_006483.2:n.594+39_594+40delinsTA