Canonical Allele Identifier: CA349369393
Gene: HOXD10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118965T>G , CM000664.2:g.176118965T>G GRCh38
NC_000002.11:g.176983693T>G , CM000664.1:g.176983693T>G GRCh37
NC_000002.10:g.176691939T>G NCBI36
NG_008133.2:g.12202T>G , LRG_246:g.12202T>G
NG_009225.1:g.1281T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.757T>G MANE Select ENSP00000249501.4:p.Ser253Ala
ENST00000249501.4:c.757T>G ENSP00000249501.4:p.Ser253Ala
ENST00000490088.2:n.581T>G
ENST00000549469.1:n.628T>G
NM_002148.3:c.757T>G , LRG_246t1:c.757T>G NP_002139.2:p.Ser253Ala
NM_002148.4:c.757T>G MANE Select NP_002139.2:p.Ser253Ala