Canonical Allele Identifier: CA1362750255

Gene: DHX30

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47848335A= , CM000665.2:g.47848335A=	GRCh38
NC_000003.11:g.47889825A= , CM000665.1:g.47889825A=	GRCh37
NC_000003.10:g.47864829A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445061.6:c.2442A= MANE Select	ENSP00000405620.1:p.Thr814=
ENST00000348968.8:c.2358A=	ENSP00000343442.4:p.Thr786=
ENST00000395745.6:c.*2342A=	ENSP00000379094.2:n.*2342A=
ENST00000445061.5:c.2442A=	ENSP00000405620.1:p.Thr814=
ENST00000446256.6:c.2442A=	ENSP00000392601.3:p.Thr814=
ENST00000457607.1:c.2526A=	ENSP00000394682.1:p.Thr842=
ENST00000474183.1:n.559A=
ENST00000619982.4:c.2325A=	ENSP00000483160.1:p.Thr775=
NM_014966.3:c.2325A=	NP_055781.2:p.Thr775=
NM_138615.2:c.2442A=	NP_619520.1:p.Thr814=
XM_006713033.1:c.2346A=	XP_006713096.1:p.Thr782=
XM_011533490.1:c.2655A=	XP_011531792.1:p.Thr885=
XM_011533491.1:c.2655A=	XP_011531793.1:p.Thr885=
XM_011533492.1:c.2655A=	XP_011531794.1:p.Thr885=
XM_011533493.1:c.2544A=	XP_011531795.1:p.Thr848=
XM_011533494.1:c.2442A=	XP_011531796.1:p.Thr814=
XM_011533495.1:c.2442A=	XP_011531797.1:p.Thr814=
XM_011533496.1:c.2358A=	XP_011531798.1:p.Thr786=
XM_011533497.1:c.2358A=	XP_011531799.1:p.Thr786=
XM_011533498.1:c.2358A=	XP_011531800.1:p.Thr786=
NM_001330990.1:c.2358A=	NP_001317919.1:p.Thr786=
XM_011533490.2:c.2655A=	XP_011531792.1:p.Thr885=
XM_011533494.3:c.2442A=	XP_011531796.1:p.Thr814=
XM_011533495.2:c.2442A=	XP_011531797.1:p.Thr814=
XM_011533497.2:c.2358A=	XP_011531799.1:p.Thr786=
XM_017005914.1:c.2574A=	XP_016861403.1:p.Thr858=
XM_017005915.1:c.2346A=	XP_016861404.1:p.Thr782=
XM_017005916.2:c.2331A=	XP_016861405.1:p.Thr777=
XM_017005917.1:c.2325A=	XP_016861406.1:p.Thr775=
XM_024453405.1:c.2544A=	XP_024309173.1:p.Thr848=
NM_138615.3:c.2442A= MANE Select	NP_619520.1:p.Thr814=
NM_001330990.2:c.2358A=	NP_001317919.1:p.Thr786=
NM_014966.4:c.2325A=	NP_055781.2:p.Thr775=