Canonical Allele Identifier: CA2667114972
Gene: TMEM39A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119431906_119431907insAGATATTTA , CM000665.2:g.119431906_119431907insAGATATTTA GRCh38
NC_000003.11:g.119150753_119150754insAGATATTTA , CM000665.1:g.119150753_119150754insAGATATTTA GRCh37
NC_000003.10:g.120633443_120633444insAGATATTTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000319172.10:c.*81_*82insCTTAAATAT MANE Select ENSP00000326063.5:n.*81_*82insCTTAAATAT
ENST00000319172.9:c.*81_*82insCTTAAATAT ENSP00000326063.5:n.*81_*82insCTTAAATAT
ENST00000438581.6:c.*1216_*1217insCTTAAATAT ENSP00000402149.2:n.*1216_*1217insCTTAAATAT
ENST00000473684.5:c.643_644insCTTAAATAT ENSP00000420432.1:n.643_644insCTTAAATAT
NM_018266.2:c.*81_*82insCTTAAATAT NP_060736.1:n.*81_*82insCTTAAATAT
NR_073506.1:n.2078_2079insCTTAAATAT
XM_005247578.1:c.*293_*294insCTTAAATAT XP_005247635.1:n.*293_*294insCTTAAATAT
XM_006713687.1:c.*81_*82insCTTAAATAT XP_006713750.1:n.*81_*82insCTTAAATAT
XM_005247578.2:c.*293_*294insCTTAAATAT XP_005247635.1:n.*293_*294insCTTAAATAT
XM_006713687.2:c.*81_*82insCTTAAATAT XP_006713750.1:n.*81_*82insCTTAAATAT
XM_017006788.2:c.*81_*82insCTTAAATAT XP_016862277.1:n.*81_*82insCTTAAATAT
XR_001740197.2:n.2100_2101insCTTAAATAT
XR_001740198.2:n.2016_2017insCTTAAATAT
NM_018266.3:c.*81_*82insCTTAAATAT MANE Select NP_060736.1:n.*81_*82insCTTAAATAT
NR_073506.2:n.2011_2012insCTTAAATAT