Canonical Allele Identifier: CA2555092888
Gene: HOXA13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198187T>C , CM000669.2:g.27198187T>C GRCh38
NC_000007.13:g.27237806T>C , CM000669.1:g.27237806T>C GRCh37
NC_000007.12:g.27204331T>C NCBI36
NG_008181.1:g.6920A>G
NG_008181.2:g.6920A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*11A>G MANE Select ENSP00000497112.1:n.*11A>G
ENST00000222753.5:c.*11A>G ENSP00000222753.4:n.*11A>G
NM_000522.4:c.*11A>G NP_000513.2:n.*11A>G
XM_011515344.1:c.*11A>G XP_011513646.1:n.*11A>G
NM_000522.5:c.*11A>G MANE Select NP_000513.2:n.*11A>G