Canonical Allele Identifier: CA351534494
Gene: TMEM43 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14130829C>T , CM000665.2:g.14130829C>T GRCh38
NC_000003.11:g.14172329C>T , CM000665.1:g.14172329C>T GRCh37
NC_000003.10:g.14147330C>T NCBI36
NG_008975.1:g.10890C>T , LRG_435:g.10890C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*200C>T ENSP00000395617.1:n.*200C>T
ENST00000306077.5:c.170C>T MANE Select ENSP00000303992.5:p.Ala57Val
ENST00000306077.4:c.170C>T ENSP00000303992.4:p.Ala57Val
ENST00000432444.1:c.*200C>T ENSP00000395617.1:n.*200C>T
NM_024334.2:c.170C>T , LRG_435t1:c.170C>T NP_077310.1:p.Ala57Val
XM_011534109.1:c.65C>T XP_011532411.1:p.Ala22Val
XM_017007176.2:c.65C>T XP_016862665.1:p.Ala22Val
NM_024334.3:c.170C>T MANE Select NP_077310.1:p.Ala57Val