Canonical Allele Identifier: CA2830538527

Gene: DHX29

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55275148_55275149del , CM000667.2:g.55275148_55275149del	GRCh38
NC_000005.9:g.54570976_54570977del , CM000667.1:g.54570976_54570977del	GRCh37
NC_000005.8:g.54606733_54606734del	NCBI36
NG_051592.1:g.37575_37576del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251636.10:c.2428-138_2428-137del MANE Select	ENSP00000251636.5:n.2428-138_2428-137del
ENST00000251636.9:c.2428-138_2428-137del	ENSP00000251636.5:n.2428-138_2428-137del
ENST00000504778.5:n.2636-138_2636-137del
ENST00000513447.1:n.96-138_96-137del
ENST00000621106.4:c.2428-138_2428-137del	ENSP00000481966.1:n.2428-138_2428-137del
NM_019030.2:c.2428-138_2428-137del	NP_061903.2:n.2428-138_2428-137del
XM_005248544.2:c.2428-138_2428-137del	XP_005248601.1:n.2428-138_2428-137del
XM_006714653.1:c.2275-138_2275-137del	XP_006714716.1:n.2275-138_2275-137del
XM_011543494.1:c.2428-138_2428-137del	XP_011541796.1:n.2428-138_2428-137del
NM_001345964.1:c.2275-138_2275-137del	NP_001332893.1:n.2275-138_2275-137del
NM_001345965.1:c.520-138_520-137del	NP_001332894.1:n.520-138_520-137del
NM_019030.3:c.2428-138_2428-137del	NP_061903.2:n.2428-138_2428-137del
NR_144323.1:n.2577-138_2577-137del
NR_144324.1:n.2577-138_2577-137del
NR_144325.1:n.2424-138_2424-137del
XR_001742128.2:n.2546-138_2546-137del
NM_019030.4:c.2428-138_2428-137del MANE Select	NP_061903.2:n.2428-138_2428-137del
NM_001345964.2:c.2275-138_2275-137del	NP_001332893.1:n.2275-138_2275-137del
NM_001345965.2:c.520-138_520-137del	NP_001332894.1:n.520-138_520-137del
NR_144323.2:n.2549-138_2549-137del
NR_144324.2:n.2549-138_2549-137del
NR_144325.2:n.2396-138_2396-137del