Canonical Allele Identifier: CA1920298988

Gene: DUSP29

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.75049002C= , CM000672.2:g.75049002C=	GRCh38
NC_000010.10:g.76808760C= , CM000672.1:g.76808760C=	GRCh37
NC_000010.9:g.76478766C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001003892.3:c.201-4985G= MANE Select	NP_001003892.1:n.201-4985G=
ENST00000338487.6:c.201-4985G= MANE Select	ENSP00000340609.5:n.201-4985G=
NM_001003892.1:c.201-4985G=	NP_001003892.1:n.201-4985G=
NM_001003892.2:c.201-4985G=	NP_001003892.1:n.201-4985G=
NM_001384909.1:c.201-4985G=	NP_001371838.1:n.201-4985G=
ENST00000338487.5:c.201-4985G=	ENSP00000340609.5:n.201-4985G=
XM_005269762.2:c.201-4985G=	XP_005269819.1:n.201-4985G=
XM_011539747.1:c.201-4985G=	XP_011538049.1:n.201-4985G=
XM_011539747.2:c.201-4985G=	XP_011538049.1:n.201-4985G=
XM_017016176.1:c.201-4180G=	XP_016871665.1:n.201-4180G=