Canonical Allele Identifier: CA2682147495
Gene: HOXA13 HGNC NCBI

Linked Data

gnomAD v4: 7-27198081-T-TCCC
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198081_27198082insCCC , CM000669.2:g.27198081_27198082insCCC GRCh38
NC_000007.13:g.27237700_27237701insCCC , CM000669.1:g.27237700_27237701insCCC GRCh37
NC_000007.12:g.27204225_27204226insCCC NCBI36
NG_008181.1:g.7025_7026insGGG
NG_008181.2:g.7025_7026insGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.*116_*117insGGG MANE Select ENSP00000497112.1:n.*116_*117insGGG
ENST00000222753.5:c.*116_*117insGGG ENSP00000222753.4:n.*116_*117insGGG
NM_000522.4:c.*116_*117insGGG NP_000513.2:n.*116_*117insGGG
XM_011515344.1:c.*116_*117insGGG XP_011513646.1:n.*116_*117insGGG
NM_000522.5:c.*116_*117insGGG MANE Select NP_000513.2:n.*116_*117insGGG
Search 100 bp 5'
Search 100 bp 3'