Canonical Allele Identifier: CA537975560

Gene: HOXD10

Linked Data

• dbSNP Id: rs1559118269
• gnomAD v2: 2-176983610-A-AAAACC
• gnomAD v3: 2-176118882-A-AAAACC
• gnomAD v4: 2-176118882-A-AAAACC
• MyVariant Identifiers: chr2:g.176983610_176983611insAAACC (hg19) ; chr2:g.176118882_176118883insAAACC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.176118885_176118886insCCAAA , CM000664.2:g.176118885_176118886insCCAAA	GRCh38
NC_000002.11:g.176983613_176983614insCCAAA , CM000664.1:g.176983613_176983614insCCAAA	GRCh37
NC_000002.10:g.176691859_176691860insCCAAA	NCBI36
NG_008133.2:g.12122_12123insCCAAA , LRG_246:g.12122_12123insCCAAA
NG_009225.1:g.1201_1202insCCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249501.5:c.746-69_746-68insCCAAA MANE Select	ENSP00000249501.4:n.746-69_746-68insCCAAA
ENST00000249501.4:c.746-69_746-68insCCAAA	ENSP00000249501.4:n.746-69_746-68insCCAAA
ENST00000490088.2:n.570-69_570-68insCCAAA
ENST00000549469.1:n.617-69_617-68insCCAAA
NM_002148.3:c.746-69_746-68insCCAAA , LRG_246t1:c.746-69_746-68insCCAAA	NP_002139.2:n.746-69_746-68insCCAAA
NM_002148.4:c.746-69_746-68insCCAAA MANE Select	NP_002139.2:n.746-69_746-68insCCAAA