Canonical Allele Identifier: CA1396556415

Gene: TMEM39A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119431989C= , CM000665.2:g.119431989C=	GRCh38
NC_000003.11:g.119150836C= , CM000665.1:g.119150836C=	GRCh37
NC_000003.10:g.120633526C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018266.3:c.1459G= MANE Select	NP_060736.1:p.Ala487=
ENST00000319172.10:c.1459G= MANE Select	ENSP00000326063.5:p.Ala487=
NM_018266.2:c.1459G=	NP_060736.1:p.Ala487=
NR_073506.1:n.1989G=
NR_073506.2:n.1922G=
ENST00000319172.9:c.1459G=	ENSP00000326063.5:p.Ala487=
ENST00000438581.6:c.*1127G=	ENSP00000402149.2:n.*1127G=
ENST00000473684.5:c.554G=	ENSP00000420432.1:n.554G=
XM_005247578.1:c.*204G=	XP_005247635.1:n.*204G=
XM_005247578.2:c.*204G=	XP_005247635.1:n.*204G=
XM_006713687.1:c.1459G=	XP_006713750.1:p.Ala487=
XM_006713687.2:c.1459G=	XP_006713750.1:p.Ala487=
XM_017006788.2:c.1375G=	XP_016862277.1:p.Ala459=
XR_001740197.2:n.2011G=
XR_001740198.2:n.1927G=