Canonical Allele Identifier: CA1362750431

Gene: DHX30

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47848745A= , CM000665.2:g.47848745A=	GRCh38
NC_000003.11:g.47890235A= , CM000665.1:g.47890235A=	GRCh37
NC_000003.10:g.47865239A=	NCBI36
NG_052840.1:g.245535T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445061.6:c.2697A= MANE Select	ENSP00000405620.1:p.Leu899=
ENST00000348968.8:c.2613A=	ENSP00000343442.4:p.Leu871=
ENST00000395745.6:c.*2597A=	ENSP00000379094.2:n.*2597A=
ENST00000445061.5:c.2697A=	ENSP00000405620.1:p.Leu899=
ENST00000446256.6:c.2697A=	ENSP00000392601.3:p.Leu899=
ENST00000457607.1:c.2781A=	ENSP00000394682.1:p.Leu927=
ENST00000474183.1:n.814A=
ENST00000619982.4:c.2580A=	ENSP00000483160.1:p.Leu860=
NM_014966.3:c.2580A=	NP_055781.2:p.Leu860=
NM_138615.2:c.2697A=	NP_619520.1:p.Leu899=
XM_006713033.1:c.2601A=	XP_006713096.1:p.Leu867=
XM_011533490.1:c.2910A=	XP_011531792.1:p.Leu970=
XM_011533491.1:c.2910A=	XP_011531793.1:p.Leu970=
XM_011533492.1:c.2910A=	XP_011531794.1:p.Leu970=
XM_011533493.1:c.2799A=	XP_011531795.1:p.Leu933=
XM_011533494.1:c.2697A=	XP_011531796.1:p.Leu899=
XM_011533495.1:c.2697A=	XP_011531797.1:p.Leu899=
XM_011533496.1:c.2613A=	XP_011531798.1:p.Leu871=
XM_011533497.1:c.2613A=	XP_011531799.1:p.Leu871=
XM_011533498.1:c.2613A=	XP_011531800.1:p.Leu871=
NM_001330990.1:c.2613A=	NP_001317919.1:p.Leu871=
XM_011533490.2:c.2910A=	XP_011531792.1:p.Leu970=
XM_011533494.3:c.2697A=	XP_011531796.1:p.Leu899=
XM_011533495.2:c.2697A=	XP_011531797.1:p.Leu899=
XM_011533497.2:c.2613A=	XP_011531799.1:p.Leu871=
XM_017005914.1:c.2829A=	XP_016861403.1:p.Leu943=
XM_017005915.1:c.2601A=	XP_016861404.1:p.Leu867=
XM_017005916.2:c.2586A=	XP_016861405.1:p.Leu862=
XM_017005917.1:c.2580A=	XP_016861406.1:p.Leu860=
XM_024453405.1:c.2799A=	XP_024309173.1:p.Leu933=
NM_138615.3:c.2697A= MANE Select	NP_619520.1:p.Leu899=
NM_001330990.2:c.2613A=	NP_001317919.1:p.Leu871=
NM_014966.4:c.2580A=	NP_055781.2:p.Leu860=