Canonical Allele Identifier: CA432552626

Gene: TMEM43

Linked Data

• MyVariant Identifiers: chr3:g.14180757C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14139257C>T , CM000665.2:g.14139257C>T	GRCh38
NC_000003.11:g.14180757C>T , CM000665.1:g.14180757C>T	GRCh37
NC_000003.10:g.14155758C>T	NCBI36
NG_008975.1:g.19318C>T , LRG_435:g.19318C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432444.2:c.*990C>T	ENSP00000395617.1:n.*990C>T
ENST00000306077.5:c.960C>T MANE Select	ENSP00000303992.5:p.Phe320=
ENST00000306077.4:c.960C>T	ENSP00000303992.4:p.Phe320=
ENST00000601399.3:n.287C>T
ENST00000608606.1:c.196C>T
NM_024334.2:c.960C>T , LRG_435t1:c.960C>T	NP_077310.1:p.Phe320=
XM_011534109.1:c.855C>T	XP_011532411.1:p.Phe285=
XM_017007176.2:c.855C>T	XP_016862665.1:p.Phe285=
NM_024334.3:c.960C>T MANE Select	NP_077310.1:p.Phe320=