Canonical Allele Identifier: CA1696263144
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs1784028346

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198191del , CM000669.2:g.27198191del GRCh38
NC_000007.13:g.27237810del , CM000669.1:g.27237810del GRCh37
NC_000007.12:g.27204335del NCBI36
NG_008181.1:g.6920del
NG_008181.2:g.6920del

Transcript Alleles

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