Canonical Allele Identifier: CA2664568578

Gene: TMEM43

Linked Data

• gnomAD v4: 3-14129409-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14129410dup , CM000665.2:g.14129410dup	GRCh38
NC_000003.11:g.14170910dup , CM000665.1:g.14170910dup	GRCh37
NC_000003.10:g.14145911dup	NCBI36
NG_008975.1:g.9471dup , LRG_435:g.9471dup

Transcript Alleles

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