Canonical Allele Identifier: CA8159880

Gene: DHX38

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72096304C>G , CM000678.2:g.72096304C>G	GRCh38
NC_000016.9:g.72130203C>G , CM000678.1:g.72130203C>G	GRCh37
NC_000016.8:g.70687704C>G	NCBI36
NG_034207.1:g.7589C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268482.8:c.147C>G MANE Select	ENSP00000268482.3:p.Leu49=
ENST00000268482.7:c.147C>G	ENSP00000268482.3:p.Leu49=
ENST00000566489.1:c.147C>G	ENSP00000457887.1:p.Leu49=
ENST00000566794.5:c.147C>G	ENSP00000455939.1:p.Leu49=
ENST00000579387.5:c.147C>G	ENSP00000462149.1:p.Leu49=
NM_014003.3:c.147C>G	NP_054722.2:p.Leu49=
XM_005256269.1:c.147C>G	XP_005256326.1:p.Leu49=
XM_011523484.1:c.147C>G	XP_011521786.1:p.Leu49=
XM_011523485.1:c.147C>G	XP_011521787.1:p.Leu49=
XR_429741.1:n.429C>G
XM_005256269.2:c.147C>G	XP_005256326.1:p.Leu49=
XM_011523484.2:c.147C>G	XP_011521786.1:p.Leu49=
XM_017023913.2:c.147C>G	XP_016879402.1:p.Leu49=
XR_429741.3:n.323C>G
NM_014003.4:c.147C>G MANE Select	NP_054722.2:p.Leu49=