Canonical Allele Identifier: CA352590598
Gene: DHX30 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47848300A>T , CM000665.2:g.47848300A>T GRCh38
NC_000003.11:g.47889790A>T , CM000665.1:g.47889790A>T GRCh37
NC_000003.10:g.47864794A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000445061.6:c.2407A>T MANE Select ENSP00000405620.1:p.Met803Leu
ENST00000348968.8:c.2323A>T ENSP00000343442.4:p.Met775Leu
ENST00000395745.6:c.*2307A>T ENSP00000379094.2:n.*2307A>T
ENST00000445061.5:c.2407A>T ENSP00000405620.1:p.Met803Leu
ENST00000446256.6:c.2407A>T ENSP00000392601.3:p.Met803Leu
ENST00000457607.1:c.2491A>T ENSP00000394682.1:p.Met831Leu
ENST00000474183.1:n.524A>T
ENST00000619982.4:c.2290A>T ENSP00000483160.1:p.Met764Leu
NM_014966.3:c.2290A>T NP_055781.2:p.Met764Leu
NM_138615.2:c.2407A>T NP_619520.1:p.Met803Leu
XM_006713033.1:c.2311A>T XP_006713096.1:p.Met771Leu
XM_011533490.1:c.2620A>T XP_011531792.1:p.Met874Leu
XM_011533491.1:c.2620A>T XP_011531793.1:p.Met874Leu
XM_011533492.1:c.2620A>T XP_011531794.1:p.Met874Leu
XM_011533493.1:c.2509A>T XP_011531795.1:p.Met837Leu
XM_011533494.1:c.2407A>T XP_011531796.1:p.Met803Leu
XM_011533495.1:c.2407A>T XP_011531797.1:p.Met803Leu
XM_011533496.1:c.2323A>T XP_011531798.1:p.Met775Leu
XM_011533497.1:c.2323A>T XP_011531799.1:p.Met775Leu
XM_011533498.1:c.2323A>T XP_011531800.1:p.Met775Leu
NM_001330990.1:c.2323A>T NP_001317919.1:p.Met775Leu
XM_011533490.2:c.2620A>T XP_011531792.1:p.Met874Leu
XM_011533494.3:c.2407A>T XP_011531796.1:p.Met803Leu
XM_011533495.2:c.2407A>T XP_011531797.1:p.Met803Leu
XM_011533497.2:c.2323A>T XP_011531799.1:p.Met775Leu
XM_017005914.1:c.2539A>T XP_016861403.1:p.Met847Leu
XM_017005915.1:c.2311A>T XP_016861404.1:p.Met771Leu
XM_017005916.2:c.2296A>T XP_016861405.1:p.Met766Leu
XM_017005917.1:c.2290A>T XP_016861406.1:p.Met764Leu
XM_024453405.1:c.2509A>T XP_024309173.1:p.Met837Leu
NM_138615.3:c.2407A>T MANE Select NP_619520.1:p.Met803Leu
NM_001330990.2:c.2323A>T NP_001317919.1:p.Met775Leu
NM_014966.4:c.2290A>T NP_055781.2:p.Met764Leu