Canonical Allele Identifier: CA2577861410

Gene: TMEM39A

Linked Data

• gnomAD v4: 3-119431898-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119431898A>T , CM000665.2:g.119431898A>T	GRCh38
NC_000003.11:g.119150745A>T , CM000665.1:g.119150745A>T	GRCh37
NC_000003.10:g.120633435A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000319172.10:c.*83T>A MANE Select	ENSP00000326063.5:n.*83T>A
ENST00000319172.9:c.*83T>A	ENSP00000326063.5:n.*83T>A
ENST00000438581.6:c.*1218T>A	ENSP00000402149.2:n.*1218T>A
ENST00000473684.5:c.645T>A	ENSP00000420432.1:n.645T>A
NM_018266.2:c.*83T>A	NP_060736.1:n.*83T>A
NR_073506.1:n.2080T>A
XM_005247578.1:c.*295T>A	XP_005247635.1:n.*295T>A
XM_006713687.1:c.*83T>A	XP_006713750.1:n.*83T>A
XM_005247578.2:c.*295T>A	XP_005247635.1:n.*295T>A
XM_006713687.2:c.*83T>A	XP_006713750.1:n.*83T>A
XM_017006788.2:c.*83T>A	XP_016862277.1:n.*83T>A
XR_001740197.2:n.2102T>A
XR_001740198.2:n.2018T>A
NM_018266.3:c.*83T>A MANE Select	NP_060736.1:n.*83T>A
NR_073506.2:n.2013T>A