Canonical Allele Identifier: CA2774817787
Gene: HOXA13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198189T>C , CM000669.2:g.27198189T>C GRCh38
NC_000007.13:g.27237808T>C , CM000669.1:g.27237808T>C GRCh37
NC_000007.12:g.27204333T>C NCBI36
NG_008181.1:g.6918A>G
NG_008181.2:g.6918A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*9A>G MANE Select ENSP00000497112.1:n.*9A>G
ENST00000222753.5:c.*9A>G ENSP00000222753.4:n.*9A>G
NM_000522.4:c.*9A>G NP_000513.2:n.*9A>G
XM_011515344.1:c.*9A>G XP_011513646.1:n.*9A>G
NM_000522.5:c.*9A>G MANE Select NP_000513.2:n.*9A>G
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