Canonical Allele Identifier: CA349369993

Gene: HOXD10

Linked Data

• MyVariant Identifiers: chr2:g.176983810A>T (hg19) ; chr2:g.176119082A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.176119082A>T , CM000664.2:g.176119082A>T	GRCh38
NC_000002.11:g.176983810A>T , CM000664.1:g.176983810A>T	GRCh37
NC_000002.10:g.176692056A>T	NCBI36
NG_008133.2:g.12319A>T , LRG_246:g.12319A>T
NG_009225.1:g.1398A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000249501.5:c.874A>T MANE Select	ENSP00000249501.4:p.Thr292Ser
ENST00000249501.4:c.874A>T	ENSP00000249501.4:p.Thr292Ser
ENST00000490088.2:n.698A>T
ENST00000549469.1:n.745A>T
NM_002148.3:c.874A>T , LRG_246t1:c.874A>T	NP_002139.2:p.Thr292Ser
NM_002148.4:c.874A>T MANE Select	NP_002139.2:p.Thr292Ser