Canonical Allele Identifier: CA367069669
Gene: HOXA13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198263T>G , CM000669.2:g.27198263T>G GRCh38
NC_000007.13:g.27237882T>G , CM000669.1:g.27237882T>G GRCh37
NC_000007.12:g.27204407T>G NCBI36
NG_008181.1:g.6844A>C
NG_008181.2:g.6844A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.1102A>C MANE Select ENSP00000497112.1:p.Ile368Leu
ENST00000222753.5:c.1102A>C ENSP00000222753.4:p.Ile368Leu
NM_000522.4:c.1102A>C NP_000513.2:p.Ile368Leu
XM_011515344.1:c.1102A>C XP_011513646.1:p.Ile368Leu
NM_000522.5:c.1102A>C MANE Select NP_000513.2:p.Ile368Leu