Canonical Allele Identifier: CA2664568025
Gene: TMEM43 HGNC NCBI

Linked Data

gnomAD v4: 3-14125095-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14125095A>C , CM000665.2:g.14125095A>C GRCh38
NC_000003.11:g.14166595A>C , CM000665.1:g.14166595A>C GRCh37
NC_000003.10:g.14141596A>C NCBI36
NG_008975.1:g.5156A>C , LRG_435:g.5156A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.-99A>C ENSP00000395617.1:n.-99A>C
ENST00000306077.5:c.-99A>C MANE Select ENSP00000303992.5:n.-99A>C
ENST00000306077.4:c.-99A>C ENSP00000303992.4:n.-99A>C
ENST00000432444.1:c.-99A>C ENSP00000395617.1:n.-99A>C
NM_024334.2:c.-99A>C , LRG_435t1:c.-99A>C NP_077310.1:n.-99A>C
XM_017007176.2:c.-435A>C XP_016862665.1:n.-435A>C
NM_024334.3:c.-99A>C MANE Select NP_077310.1:n.-99A>C
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