Canonical Allele Identifier: CA1696262952
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs1784026175
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198082_27198087dup , CM000669.2:g.27198082_27198087dup GRCh38
NC_000007.13:g.27237701_27237706dup , CM000669.1:g.27237701_27237706dup GRCh37
NC_000007.12:g.27204226_27204231dup NCBI36
NG_008181.1:g.7026_7031dup
NG_008181.2:g.7026_7031dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.*117_*122dup MANE Select ENSP00000497112.1:n.*117_*122dup
ENST00000222753.5:c.*117_*122dup ENSP00000222753.4:n.*117_*122dup
NM_000522.4:c.*117_*122dup NP_000513.2:n.*117_*122dup
XM_011515344.1:c.*117_*122dup XP_011513646.1:n.*117_*122dup
NM_000522.5:c.*117_*122dup MANE Select NP_000513.2:n.*117_*122dup
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