Canonical Allele Identifier: CA359752001

Gene: DHX29

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55294020G>C , CM000667.2:g.55294020G>C	GRCh38
NC_000005.9:g.54589848G>C , CM000667.1:g.54589848G>C	GRCh37
NC_000005.8:g.54625605G>C	NCBI36
NG_051592.1:g.18703C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_019030.4:c.777C>G MANE Select	NP_061903.2:p.Asp259Glu
ENST00000251636.10:c.777C>G MANE Select	ENSP00000251636.5:p.Asp259Glu
NM_001345964.1:c.777C>G	NP_001332893.1:p.Asp259Glu
NM_001345964.2:c.777C>G	NP_001332893.1:p.Asp259Glu
NM_001345965.1:c.-1219C>G	NP_001332894.1:n.-1219C>G
NM_001345965.2:c.-1219C>G	NP_001332894.1:n.-1219C>G
NM_019030.2:c.777C>G	NP_061903.2:p.Asp259Glu
NM_019030.3:c.777C>G	NP_061903.2:p.Asp259Glu
NR_144323.1:n.926C>G
NR_144323.2:n.898C>G
NR_144324.1:n.926C>G
NR_144324.2:n.898C>G
NR_144325.1:n.926C>G
NR_144325.2:n.898C>G
ENST00000251636.9:c.777C>G	ENSP00000251636.5:p.Asp259Glu
ENST00000504778.5:n.898C>G
ENST00000621106.4:c.777C>G	ENSP00000481966.1:p.Asp259Glu
XM_005248544.2:c.777C>G	XP_005248601.1:p.Asp259Glu
XM_006714653.1:c.777C>G	XP_006714716.1:p.Asp259Glu
XM_011543494.1:c.777C>G	XP_011541796.1:p.Asp259Glu
XR_001742128.2:n.895C>G
XR_001742666.1:n.80-820G>C
XR_948335.1:n.1163-820G>C
XR_948336.1:n.229-820G>C