Canonical Allele Identifier: CA430224642

Gene: HOXD13

Linked Data

• MyVariant Identifiers: chr2:g.176958293_176958294insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.176093565_176093566insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG , CM000664.2:g.176093565_176093566insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG	GRCh38
NC_000002.11:g.176958293_176958294insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG , CM000664.1:g.176958293_176958294insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG	GRCh37
NC_000002.10:g.176666539_176666540insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG	NCBI36
NG_008137.1:g.5762_5763insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392539.4:c.675_676insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG MANE Select	ENSP00000376322.3:p.Met226AlafsTer34
ENST00000392539.3:c.675_676insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG	ENSP00000376322.3:p.Met226AlafsTer34
NM_000523.3:c.675_676insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG	NP_000514.2:p.Met226AlafsTer34
XM_011511068.1:c.725-915_725-914insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG	XP_011509370.1:n.725-915_725-914insGCGGCCGAACCGAGCCTTGGATGGCG...
XM_011511068.2:c.725-915_725-914insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG	XP_011509370.1:n.725-915_725-914insGCGGCCGAACCGAGCCTTGGATGGCG...
NM_000523.4:c.675_676insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG MANE Select	NP_000514.2:p.Met226AlafsTer34