Canonical Allele Identifier: CA1309461729

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176151875A= , CM000664.2:g.176151875A= GRCh38
NC_000002.11:g.177016603A= , CM000664.1:g.177016603A= GRCh37
NC_000002.10:g.176724849A= NCBI36
NG_012080.1:g.5491A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306324.4:c.242A= (HOXD4) MANE Select ENSP00000302548.3:p.Glu81=
ENST00000306324.3:c.242A= (HOXD4) ENSP00000302548.3:p.Glu81=
ENST00000432796.2:c.-85+14876A= (HOXD3) ENSP00000392615.2:n.-85+14876A=
ENST00000468418.4:c.242A= ENSP00000424734.3:p.Glu81=
NM_014621.2:c.242A= (HOXD4) NP_055436.2:p.Glu81=
XM_005246510.3:c.-180-12198A= (HOXD3) XP_005246567.1:n.-180-12198A=
XM_005246514.3:c.242A= (HOXD4) XP_005246571.1:p.Glu81=
XM_006712477.2:c.-85+14876A= (HOXD3) XP_006712540.1:n.-85+14876A=
XM_005246514.4:c.242A= (HOXD4) XP_005246571.1:p.Glu81=
NM_014621.3:c.242A= (HOXD4) MANE Select NP_055436.2:p.Glu81=