Canonical Allele Identifier: CA352590169
Gene: DHX30 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47848198G>T , CM000665.2:g.47848198G>T GRCh38
NC_000003.11:g.47889688G>T , CM000665.1:g.47889688G>T GRCh37
NC_000003.10:g.47864692G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000445061.6:c.2305G>T MANE Select ENSP00000405620.1:p.Val769Leu
ENST00000348968.8:c.2221G>T ENSP00000343442.4:p.Val741Leu
ENST00000395745.6:c.*2205G>T ENSP00000379094.2:n.*2205G>T
ENST00000445061.5:c.2305G>T ENSP00000405620.1:p.Val769Leu
ENST00000446256.6:c.2305G>T ENSP00000392601.3:p.Val769Leu
ENST00000457607.1:c.2389G>T ENSP00000394682.1:p.Val797Leu
ENST00000474183.1:n.422G>T
ENST00000619982.4:c.2188G>T ENSP00000483160.1:p.Val730Leu
NM_014966.3:c.2188G>T NP_055781.2:p.Val730Leu
NM_138615.2:c.2305G>T NP_619520.1:p.Val769Leu
XM_006713033.1:c.2209G>T XP_006713096.1:p.Val737Leu
XM_011533490.1:c.2518G>T XP_011531792.1:p.Val840Leu
XM_011533491.1:c.2518G>T XP_011531793.1:p.Val840Leu
XM_011533492.1:c.2518G>T XP_011531794.1:p.Val840Leu
XM_011533493.1:c.2407G>T XP_011531795.1:p.Val803Leu
XM_011533494.1:c.2305G>T XP_011531796.1:p.Val769Leu
XM_011533495.1:c.2305G>T XP_011531797.1:p.Val769Leu
XM_011533496.1:c.2221G>T XP_011531798.1:p.Val741Leu
XM_011533497.1:c.2221G>T XP_011531799.1:p.Val741Leu
XM_011533498.1:c.2221G>T XP_011531800.1:p.Val741Leu
NM_001330990.1:c.2221G>T NP_001317919.1:p.Val741Leu
XM_011533490.2:c.2518G>T XP_011531792.1:p.Val840Leu
XM_011533494.3:c.2305G>T XP_011531796.1:p.Val769Leu
XM_011533495.2:c.2305G>T XP_011531797.1:p.Val769Leu
XM_011533497.2:c.2221G>T XP_011531799.1:p.Val741Leu
XM_017005914.1:c.2437G>T XP_016861403.1:p.Val813Leu
XM_017005915.1:c.2209G>T XP_016861404.1:p.Val737Leu
XM_017005916.2:c.2194G>T XP_016861405.1:p.Val732Leu
XM_017005917.1:c.2188G>T XP_016861406.1:p.Val730Leu
XM_024453405.1:c.2407G>T XP_024309173.1:p.Val803Leu
NM_138615.3:c.2305G>T MANE Select NP_619520.1:p.Val769Leu
NM_001330990.2:c.2221G>T NP_001317919.1:p.Val741Leu
NM_014966.4:c.2188G>T NP_055781.2:p.Val730Leu