Canonical Allele Identifier: CA2682147487
Gene: HOXA13 HGNC NCBI

Linked Data

gnomAD v4: 7-27198077-T-TTTC
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198077_27198078insTTC , CM000669.2:g.27198077_27198078insTTC GRCh38
NC_000007.13:g.27237696_27237697insTTC , CM000669.1:g.27237696_27237697insTTC GRCh37
NC_000007.12:g.27204221_27204222insTTC NCBI36
NG_008181.1:g.7029_7030insGAA
NG_008181.2:g.7029_7030insGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.*120_*121insGAA MANE Select ENSP00000497112.1:n.*120_*121insGAA
ENST00000222753.5:c.*120_*121insGAA ENSP00000222753.4:n.*120_*121insGAA
NM_000522.4:c.*120_*121insGAA NP_000513.2:n.*120_*121insGAA
XM_011515344.1:c.*120_*121insGAA XP_011513646.1:n.*120_*121insGAA
NM_000522.5:c.*120_*121insGAA MANE Select NP_000513.2:n.*120_*121insGAA
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