Canonical Allele Identifier: CA352593608

Gene: DHX30

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47849314G>A , CM000665.2:g.47849314G>A	GRCh38
NC_000003.11:g.47890804G>A , CM000665.1:g.47890804G>A	GRCh37
NC_000003.10:g.47865808G>A	NCBI36
NG_052840.1:g.244966C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_138615.3:c.3052G>A MANE Select	NP_619520.1:p.Val1018Met
ENST00000445061.6:c.3052G>A MANE Select	ENSP00000405620.1:p.Val1018Met
NM_001330990.1:c.2968G>A	NP_001317919.1:p.Val990Met
NM_001330990.2:c.2968G>A	NP_001317919.1:p.Val990Met
NM_014966.3:c.2935G>A	NP_055781.2:p.Val979Met
NM_014966.4:c.2935G>A	NP_055781.2:p.Val979Met
NM_138615.2:c.3052G>A	NP_619520.1:p.Val1018Met
ENST00000348968.8:c.2968G>A	ENSP00000343442.4:p.Val990Met
ENST00000395745.6:c.*2952G>A	ENSP00000379094.2:n.*2952G>A
ENST00000445061.5:c.3052G>A	ENSP00000405620.1:p.Val1018Met
ENST00000446256.6:c.3052G>A	ENSP00000392601.3:p.Val1018Met
ENST00000457607.1:c.3136G>A	ENSP00000394682.1:p.Val1046Met
ENST00000619982.4:c.2935G>A	ENSP00000483160.1:p.Val979Met
XM_006713033.1:c.2956G>A	XP_006713096.1:p.Val986Met
XM_011533490.1:c.3265G>A	XP_011531792.1:p.Val1089Met
XM_011533490.2:c.3265G>A	XP_011531792.1:p.Val1089Met
XM_011533491.1:c.3265G>A	XP_011531793.1:p.Val1089Met
XM_011533492.1:c.3265G>A	XP_011531794.1:p.Val1089Met
XM_011533493.1:c.3154G>A	XP_011531795.1:p.Val1052Met
XM_011533494.1:c.3052G>A	XP_011531796.1:p.Val1018Met
XM_011533494.3:c.3052G>A	XP_011531796.1:p.Val1018Met
XM_011533495.1:c.3052G>A	XP_011531797.1:p.Val1018Met
XM_011533495.2:c.3052G>A	XP_011531797.1:p.Val1018Met
XM_011533496.1:c.2968G>A	XP_011531798.1:p.Val990Met
XM_011533497.1:c.2968G>A	XP_011531799.1:p.Val990Met
XM_011533497.2:c.2968G>A	XP_011531799.1:p.Val990Met
XM_011533498.1:c.2968G>A	XP_011531800.1:p.Val990Met
XM_017005914.1:c.3184G>A	XP_016861403.1:p.Val1062Met
XM_017005915.1:c.2956G>A	XP_016861404.1:p.Val986Met
XM_017005916.2:c.2941G>A	XP_016861405.1:p.Val981Met
XM_017005917.1:c.2935G>A	XP_016861406.1:p.Val979Met
XM_024453405.1:c.3154G>A	XP_024309173.1:p.Val1052Met