Canonical Allele Identifier: CA351534323
Gene: TMEM43 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.14170994C>A (hg19) chr3:g.14129494C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129494C>A , CM000665.2:g.14129494C>A GRCh38
NC_000003.11:g.14170994C>A , CM000665.1:g.14170994C>A GRCh37
NC_000003.10:g.14145995C>A NCBI36
NG_008975.1:g.9555C>A , LRG_435:g.9555C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*125C>A ENSP00000395617.1:n.*125C>A
ENST00000306077.5:c.95C>A MANE Select ENSP00000303992.5:p.Thr32Asn
ENST00000306077.4:c.95C>A ENSP00000303992.4:p.Thr32Asn
ENST00000432444.1:c.*125C>A ENSP00000395617.1:n.*125C>A
NM_024334.2:c.95C>A , LRG_435t1:c.95C>A NP_077310.1:p.Thr32Asn
XM_011534109.1:c.-11C>A XP_011532411.1:n.-11C>A
XM_017007176.2:c.-11C>A XP_016862665.1:n.-11C>A
NM_024334.3:c.95C>A MANE Select NP_077310.1:p.Thr32Asn
Search 100 bp 5'
Search 100 bp 3'