Canonical Allele Identifier: CA2577861407

Gene: TMEM39A

Linked Data

• gnomAD v4: 3-119431887-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119431891del , CM000665.2:g.119431891del	GRCh38
NC_000003.11:g.119150738del , CM000665.1:g.119150738del	GRCh37
NC_000003.10:g.120633428del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000319172.10:c.*93del MANE Select	ENSP00000326063.5:n.*93del
ENST00000319172.9:c.*93del	ENSP00000326063.5:n.*93del
ENST00000438581.6:c.*1228del	ENSP00000402149.2:n.*1228del
ENST00000473684.5:c.655del	ENSP00000420432.1:n.655del
NM_018266.2:c.*93del	NP_060736.1:n.*93del
NR_073506.1:n.2090del
XM_005247578.1:c.*305del	XP_005247635.1:n.*305del
XM_006713687.1:c.*93del	XP_006713750.1:n.*93del
XM_005247578.2:c.*305del	XP_005247635.1:n.*305del
XM_006713687.2:c.*93del	XP_006713750.1:n.*93del
XM_017006788.2:c.*93del	XP_016862277.1:n.*93del
XR_001740197.2:n.2112del
XR_001740198.2:n.2028del
NM_018266.3:c.*93del MANE Select	NP_060736.1:n.*93del
NR_073506.2:n.2023del