Canonical Allele Identifier: CA051567
Gene: TMEM43 HGNC NCBI

Linked Data

dbSNP Id: rs762632835
gnomAD v2: 3-14170894-C-T
gnomAD v4: 3-14129394-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14129394C>T , CM000665.2:g.14129394C>T GRCh38
NC_000003.11:g.14170894C>T , CM000665.1:g.14170894C>T GRCh37
NC_000003.10:g.14145895C>T NCBI36
NG_008975.1:g.9455C>T , LRG_435:g.9455C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*43-18C>T ENSP00000395617.1:n.*43-18C>T
ENST00000306077.5:c.13-18C>T MANE Select ENSP00000303992.5:n.13-18C>T
ENST00000306077.4:c.13-18C>T ENSP00000303992.4:n.13-18C>T
ENST00000432444.1:c.*43-18C>T ENSP00000395617.1:n.*43-18C>T
NM_024334.2:c.13-18C>T , LRG_435t1:c.13-18C>T NP_077310.1:n.13-18C>T
XM_011534109.1:c.-93-18C>T XP_011532411.1:n.-93-18C>T
XM_017007176.2:c.-93-18C>T XP_016862665.1:n.-93-18C>T
NM_024334.3:c.13-18C>T MANE Select NP_077310.1:n.13-18C>T