Canonical Allele Identifier: CA2682147498
Gene: HOXA13 HGNC NCBI

Linked Data

gnomAD v4: 7-27198082-G-GAAGGAGA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198082_27198083insAAGGAGA , CM000669.2:g.27198082_27198083insAAGGAGA GRCh38
NC_000007.13:g.27237701_27237702insAAGGAGA , CM000669.1:g.27237701_27237702insAAGGAGA GRCh37
NC_000007.12:g.27204226_27204227insAAGGAGA NCBI36
NG_008181.1:g.7024_7025insTCTCCTT
NG_008181.2:g.7024_7025insTCTCCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*115_*116insTCTCCTT MANE Select ENSP00000497112.1:n.*115_*116insTCTCCTT
ENST00000222753.5:c.*115_*116insTCTCCTT ENSP00000222753.4:n.*115_*116insTCTCCTT
NM_000522.4:c.*115_*116insTCTCCTT NP_000513.2:n.*115_*116insTCTCCTT
XM_011515344.1:c.*115_*116insTCTCCTT XP_011513646.1:n.*115_*116insTCTCCTT
NM_000522.5:c.*115_*116insTCTCCTT MANE Select NP_000513.2:n.*115_*116insTCTCCTT
Search 100 bp 5'
Search 100 bp 3'