Canonical Allele Identifier: CA1309445409
Gene: HOXD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119185G= , CM000664.2:g.176119185G= GRCh38
NC_000002.11:g.176983913G= , CM000664.1:g.176983913G= GRCh37
NC_000002.10:g.176692159G= NCBI36
NG_008133.2:g.12422G= , LRG_246:g.12422G=
NG_009225.1:g.1501G=

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.977G= MANE Select ENSP00000249501.4:p.Arg326=
ENST00000249501.4:c.977G= ENSP00000249501.4:p.Arg326=
ENST00000490088.2:n.801G=
ENST00000549469.1:n.848G=
NM_002148.3:c.977G= , LRG_246t1:c.977G= NP_002139.2:p.Arg326=
NM_002148.4:c.977G= MANE Select NP_002139.2:p.Arg326=