Canonical Allele Identifier: CA1696262961
Gene: HOXA13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198084_27198088delinsCTCTT , CM000669.2:g.27198084_27198088delinsCTCTT GRCh38
NC_000007.13:g.27237703_27237707delinsCTCTT , CM000669.1:g.27237703_27237707delinsCTCTT GRCh37
NC_000007.12:g.27204228_27204232delinsCTCTT NCBI36
NG_008181.1:g.7019_7023delinsAAGAG
NG_008181.2:g.7019_7023delinsAAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000649031.1:c.*110_*114delinsAAGAG MANE Select ENSP00000497112.1:n.*110_*114delinsAAGAG
ENST00000222753.5:c.*110_*114delinsAAGAG ENSP00000222753.4:n.*110_*114delinsAAGAG
NM_000522.4:c.*110_*114delinsAAGAG NP_000513.2:n.*110_*114delinsAAGAG
XM_011515344.1:c.*110_*114delinsAAGAG XP_011513646.1:n.*110_*114delinsAAGAG
NM_000522.5:c.*110_*114delinsAAGAG MANE Select NP_000513.2:n.*110_*114delinsAAGAG
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