Canonical Allele Identifier: CA351536126

Gene: TMEM43

Linked Data

• MyVariant Identifiers: chr3:g.14180705G>C (hg19) ; chr3:g.14139205G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14139205G>C , CM000665.2:g.14139205G>C	GRCh38
NC_000003.11:g.14180705G>C , CM000665.1:g.14180705G>C	GRCh37
NC_000003.10:g.14155706G>C	NCBI36
NG_008975.1:g.19266G>C , LRG_435:g.19266G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000432444.2:c.*938G>C	ENSP00000395617.1:n.*938G>C
ENST00000306077.5:c.908G>C MANE Select	ENSP00000303992.5:p.Ser303Thr
ENST00000306077.4:c.908G>C	ENSP00000303992.4:p.Ser303Thr
ENST00000601399.3:n.235G>C
ENST00000608606.1:c.144G>C
NM_024334.2:c.908G>C , LRG_435t1:c.908G>C	NP_077310.1:p.Ser303Thr
XM_011534109.1:c.803G>C	XP_011532411.1:p.Ser268Thr
XM_017007176.2:c.803G>C	XP_016862665.1:p.Ser268Thr
NM_024334.3:c.908G>C MANE Select	NP_077310.1:p.Ser303Thr