Canonical Allele Identifier: CA2682147485
Gene: HOXA13 HGNC NCBI

Linked Data

gnomAD v4: 7-27198076-GTC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198080_27198081del , CM000669.2:g.27198080_27198081del GRCh38
NC_000007.13:g.27237699_27237700del , CM000669.1:g.27237699_27237700del GRCh37
NC_000007.12:g.27204224_27204225del NCBI36
NG_008181.1:g.7029_7030del
NG_008181.2:g.7029_7030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.*120_*121del MANE Select ENSP00000497112.1:n.*120_*121del
ENST00000222753.5:c.*120_*121del ENSP00000222753.4:n.*120_*121del
NM_000522.4:c.*120_*121del NP_000513.2:n.*120_*121del
XM_011515344.1:c.*120_*121del XP_011513646.1:n.*120_*121del
NM_000522.5:c.*120_*121del MANE Select NP_000513.2:n.*120_*121del
Search 100 bp 5'
Search 100 bp 3'