Canonical Allele Identifier: CA28736204
Community Standard Title: NM_006492.3(ALX3):c.*68_*69insCCTGCCTGGACACCACGGAGGAAGCACC

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110060668_110060669insCTTCCTCCGTGGTGTCCAGGCAGGGGTG , CM000663.2:g.110060668_110060669insCTTCCTCCGTGGTGTCCAGGCAGGGGTG GRCh38
NC_000001.10:g.110603290_110603291insCTTCCTCCGTGGTGTCCAGGCAGGGGTG , CM000663.1:g.110603290_110603291insCTTCCTCCGTGGTGTCCAGGCAGGGGTG GRCh37
NC_000001.9:g.110404813_110404814insCTTCCTCCGTGGTGTCCAGGCAGGGGTG NCBI36
NG_012039.1:g.15036_15037insCCTGCCTGGACACCACGGAGGAAGCACC

Transcript Alleles

HGVS Amino-acid Change
NM_006492.3:c.*68_*69insCCTGCCTGGACACCACGGAGGAAGCACC (ALX3) MANE Select NP_006483.2:n.*68_*69insCCTGCCTGGACACCACGGAGGAAGCACC
ENST00000647563.2:c.*68_*69insCCTGCCTGGACACCACGGAGGAAGCACC (ALX3) MANE Select ENSP00000497310.1:n.*68_*69insCCTGCCTGGACACCACGGAGGAAGCACC
NM_006492.2:c.*68_*69insCCTGCCTGGACACCACGGAGGAAGCACC (ALX3) NP_006483.2:n.*68_*69insCCTGCCTGGACACCACGGAGGAAGCACC
ENST00000369792.4:c.*68_*69insCCTGCCTGGACACCACGGAGGAAGCACC (ALX3) ENSP00000358807.3:n.*68_*69insCCTGCCTGGACACCACGGAGGAAGCACC
ENST00000473429.5:n.4213+5866_4213+5867insCTTCCTCCGTGGTGTCCAGGCAGGGGTG (STRIP1)
ENST00000649954.1:c.*68_*69insCCTGCCTGGACACCACGGAGGAAGCACC (ALX3) ENSP00000497035.1:n.*68_*69insCCTGCCTGGACACCACGGAGGAAGCACC