Canonical Allele Identifier: CA69738042

Gene: TMEM43

Linked Data

• dbSNP Id: rs976219937
• MyVariant Identifiers: chr3:g.14141423T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14141423T>G , CM000665.2:g.14141423T>G	GRCh38
NC_000003.11:g.14182923T>G , CM000665.1:g.14182923T>G	GRCh37
NC_000003.10:g.14157924T>G	NCBI36
NG_008975.1:g.21484T>G , LRG_435:g.21484T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432444.2:c.*1031-170T>G	ENSP00000395617.1:n.*1031-170T>G
ENST00000306077.5:c.1001-170T>G MANE Select	ENSP00000303992.5:n.1001-170T>G
ENST00000306077.4:c.1001-170T>G	ENSP00000303992.4:n.1001-170T>G
ENST00000601399.3:n.327+2126T>G
ENST00000608606.1:c.236+2126T>G
NM_024334.2:c.1001-170T>G , LRG_435t1:c.1001-170T>G	NP_077310.1:n.1001-170T>G
XM_011534109.1:c.896-170T>G	XP_011532411.1:n.896-170T>G
XM_017007176.2:c.896-170T>G	XP_016862665.1:n.896-170T>G
NM_024334.3:c.1001-170T>G MANE Select	NP_077310.1:n.1001-170T>G