Canonical Allele Identifier: CA1309469860

Gene: HOXD3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.176169393G= , CM000664.2:g.176169393G=	GRCh38
NC_000002.11:g.177034121G= , CM000664.1:g.177034121G=	GRCh37
NC_000002.10:g.176742367G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006898.5:c.279G= MANE Select	NP_008829.3:p.Pro93=
ENST00000683222.1:c.279G= MANE Select	ENSP00000507129.1:p.Pro93=
NM_006898.4:c.279G=	NP_008829.3:p.Pro93=
ENST00000249440.4:c.279G=	ENSP00000249440.2:p.Pro93=
ENST00000410016.5:c.279G=	ENSP00000386498.1:p.Pro93=
ENST00000432796.2:c.279G=	ENSP00000392615.2:p.Pro93=
ENST00000468418.4:c.*688G=	ENSP00000424734.3:n.*688G=
XM_005246509.2:c.279G=	XP_005246566.1:p.Pro93=
XM_005246509.4:c.279G=	XP_005246566.1:p.Pro93=
XM_005246510.3:c.279G=	XP_005246567.1:p.Pro93=
XM_005246511.2:c.279G=	XP_005246568.1:p.Pro93=
XM_005246511.4:c.279G=	XP_005246568.1:p.Pro93=
XM_005246513.3:c.279G=	XP_005246570.1:p.Pro93=
XM_005246513.5:c.279G=	XP_005246570.1:p.Pro93=
XM_006712477.2:c.279G=	XP_006712540.1:p.Pro93=
XM_011511065.1:c.279G=	XP_011509367.1:p.Pro93=
XM_011511065.3:c.279G=	XP_011509367.1:p.Pro93=
XM_011511066.1:c.279G=	XP_011509368.1:p.Pro93=
XM_011511066.3:c.279G=	XP_011509368.1:p.Pro93=