Canonical Allele Identifier: CA2702106591
Gene: TMEM43 HGNC NCBI

Linked Data

dbSNP Id: rs2124985437
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129392T>G , CM000665.2:g.14129392T>G GRCh38
NC_000003.11:g.14170892T>G , CM000665.1:g.14170892T>G GRCh37
NC_000003.10:g.14145893T>G NCBI36
NG_008975.1:g.9453T>G , LRG_435:g.9453T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*43-20T>G ENSP00000395617.1:n.*43-20T>G
ENST00000306077.5:c.13-20T>G MANE Select ENSP00000303992.5:n.13-20T>G
ENST00000306077.4:c.13-20T>G ENSP00000303992.4:n.13-20T>G
ENST00000432444.1:c.*43-20T>G ENSP00000395617.1:n.*43-20T>G
NM_024334.2:c.13-20T>G , LRG_435t1:c.13-20T>G NP_077310.1:n.13-20T>G
XM_011534109.1:c.-93-20T>G XP_011532411.1:n.-93-20T>G
XM_017007176.2:c.-93-20T>G XP_016862665.1:n.-93-20T>G
NM_024334.3:c.13-20T>G MANE Select NP_077310.1:n.13-20T>G
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