Canonical Allele Identifier: CA351536292

Gene: TMEM43

Linked Data

• MyVariant Identifiers: chr3:g.14180780G>C (hg19) ; chr3:g.14139280G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14139280G>C , CM000665.2:g.14139280G>C	GRCh38
NC_000003.11:g.14180780G>C , CM000665.1:g.14180780G>C	GRCh37
NC_000003.10:g.14155781G>C	NCBI36
NG_008975.1:g.19341G>C , LRG_435:g.19341G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432444.2:c.*1013G>C	ENSP00000395617.1:n.*1013G>C
ENST00000306077.5:c.983G>C MANE Select	ENSP00000303992.5:p.Arg328Pro
ENST00000306077.4:c.983G>C	ENSP00000303992.4:p.Arg328Pro
ENST00000601399.3:n.310G>C
ENST00000608606.1:c.219G>C
NM_024334.2:c.983G>C , LRG_435t1:c.983G>C	NP_077310.1:p.Arg328Pro
XM_011534109.1:c.878G>C	XP_011532411.1:p.Arg293Pro
XM_017007176.2:c.878G>C	XP_016862665.1:p.Arg293Pro
NM_024334.3:c.983G>C MANE Select	NP_077310.1:p.Arg328Pro