Canonical Allele Identifier: CA913089434

Gene: HOXD13

Linked Data

• MyVariant Identifiers: chr2:g.176958308_176958311del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.176093580_176093583del , CM000664.2:g.176093580_176093583del	GRCh38
NC_000002.11:g.176958308_176958311del , CM000664.1:g.176958308_176958311del	GRCh37
NC_000002.10:g.176666554_176666557del	NCBI36
NG_008137.1:g.5777_5780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392539.4:c.690_693del MANE Select	ENSP00000376322.3:p.Gln230HisfsTer?
ENST00000392539.3:c.690_693del	ENSP00000376322.3:p.Gln230HisfsTer?
NM_000523.3:c.690_693del	NP_000514.2:p.Gln230HisfsTer?
XM_011511068.1:c.725-900_725-897del	XP_011509370.1:n.725-900_725-897del
XM_011511068.2:c.725-900_725-897del	XP_011509370.1:n.725-900_725-897del
NM_000523.4:c.690_693del MANE Select	NP_000514.2:p.Gln230HisfsTer?