Canonical Allele Identifier: CA573759157
Community Standard Title: NM_000522.5(HOXA13):c.351_377del (p.Ala125_Ala133del)
Gene: HOXA13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27199706_27199732del , CM000669.2:g.27199706_27199732del GRCh38
NC_000007.13:g.27239325_27239351del , CM000669.1:g.27239325_27239351del GRCh37
NC_000007.12:g.27205850_27205876del NCBI36
NG_008181.1:g.5380_5406del
NG_008181.2:g.5380_5406del

Transcript Alleles

HGVS Amino-acid Change
NM_000522.5:c.351_377del MANE Select NP_000513.2:p.Ala118_Ala126del
ENST00000649031.1:c.351_377del MANE Select ENSP00000497112.1:p.Ala118_Ala126del
NM_000522.4:c.351_377del NP_000513.2:p.Ala118_Ala126del
ENST00000222753.5:c.351_377del ENSP00000222753.4:p.Ala118_Ala126del
XM_011515344.1:c.351_377del XP_011513646.1:p.Ala118_Ala126del
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