Canonical Allele Identifier: CA1309461300

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176151087C= , CM000664.2:g.176151087C= GRCh38
NC_000002.11:g.177015815C= , CM000664.1:g.177015815C= GRCh37
NC_000002.10:g.176724061C= NCBI36
NG_012080.1:g.4703C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432796.2:c.-85+14088C= (HOXD3) ENSP00000392615.2:n.-85+14088C=
ENST00000468418.4:c.-547C= ENSP00000424734.3:n.-547C=
XM_005246510.3:c.-180-12986C= (HOXD3) XP_005246567.1:n.-180-12986C=
XM_005246514.3:c.-547C= (HOXD4) XP_005246571.1:n.-547C=
XM_005246514.4:c.-547C= (HOXD4) XP_005246571.1:n.-547C=
XM_006712477.2:c.-85+14088C= (HOXD3) XP_006712540.1:n.-85+14088C=