Canonical Allele Identifier: CA351536409
Gene: TMEM43 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14141626A>T , CM000665.2:g.14141626A>T GRCh38
NC_000003.11:g.14183126A>T , CM000665.1:g.14183126A>T GRCh37
NC_000003.10:g.14158127A>T NCBI36
NG_008975.1:g.21687A>T , LRG_435:g.21687A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*1064A>T ENSP00000395617.1:n.*1064A>T
ENST00000306077.5:c.1034A>T MANE Select ENSP00000303992.5:p.Asn345Ile
ENST00000306077.4:c.1034A>T ENSP00000303992.4:p.Asn345Ile
ENST00000601399.3:n.327+2329A>T
ENST00000608606.1:c.236+2329A>T
NM_024334.2:c.1034A>T , LRG_435t1:c.1034A>T NP_077310.1:p.Asn345Ile
XM_011534109.1:c.929A>T XP_011532411.1:p.Asn310Ile
XM_017007176.2:c.929A>T XP_016862665.1:p.Asn310Ile
NM_024334.3:c.1034A>T MANE Select NP_077310.1:p.Asn345Ile