Canonical Allele Identifier: CA432551082
Gene: TMEM43 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.14172327C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14130827C>G , CM000665.2:g.14130827C>G GRCh38
NC_000003.11:g.14172327C>G , CM000665.1:g.14172327C>G GRCh37
NC_000003.10:g.14147328C>G NCBI36
NG_008975.1:g.10888C>G , LRG_435:g.10888C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*198C>G ENSP00000395617.1:n.*198C>G
ENST00000306077.5:c.168C>G MANE Select ENSP00000303992.5:p.Arg56=
ENST00000306077.4:c.168C>G ENSP00000303992.4:p.Arg56=
ENST00000432444.1:c.*198C>G ENSP00000395617.1:n.*198C>G
NM_024334.2:c.168C>G , LRG_435t1:c.168C>G NP_077310.1:p.Arg56=
XM_011534109.1:c.63C>G XP_011532411.1:p.Arg21=
XM_017007176.2:c.63C>G XP_016862665.1:p.Arg21=
NM_024334.3:c.168C>G MANE Select NP_077310.1:p.Arg56=
Search 100 bp 5'
Search 100 bp 3'