Canonical Allele Identifier: CA2682147424
Gene: HOXA13 HGNC NCBI

Linked Data

gnomAD v4: 7-27198052-CTCCTTCGGG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198053_27198061del , CM000669.2:g.27198053_27198061del GRCh38
NC_000007.13:g.27237672_27237680del , CM000669.1:g.27237672_27237680del GRCh37
NC_000007.12:g.27204197_27204205del NCBI36
NG_008181.1:g.7046_7054del
NG_008181.2:g.7046_7054del

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*137_*145del MANE Select ENSP00000497112.1:n.*137_*145del
ENST00000222753.5:c.*137_*145del ENSP00000222753.4:n.*137_*145del
NM_000522.4:c.*137_*145del NP_000513.2:n.*137_*145del
XM_011515344.1:c.*137_*145del XP_011513646.1:n.*137_*145del
NM_000522.5:c.*137_*145del MANE Select NP_000513.2:n.*137_*145del
Search 100 bp 5'
Search 100 bp 3'