Canonical Allele Identifier: CA351533962

Gene: TMEM43

Linked Data

• MyVariant Identifiers: chr3:g.14166697G>T (hg19) ; chr3:g.14125197G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14125197G>T , CM000665.2:g.14125197G>T	GRCh38
NC_000003.11:g.14166697G>T , CM000665.1:g.14166697G>T	GRCh37
NC_000003.10:g.14141698G>T	NCBI36
NG_008975.1:g.5258G>T , LRG_435:g.5258G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000432444.2:c.4G>T	ENSP00000395617.1:p.Ala2Ser
ENST00000306077.5:c.4G>T MANE Select	ENSP00000303992.5:p.Ala2Ser
ENST00000306077.4:c.4G>T	ENSP00000303992.4:p.Ala2Ser
ENST00000432444.1:c.4G>T	ENSP00000395617.1:p.Ala2Ser
NM_024334.2:c.4G>T , LRG_435t1:c.4G>T	NP_077310.1:p.Ala2Ser
XM_017007176.2:c.-333G>T	XP_016862665.1:n.-333G>T
NM_024334.3:c.4G>T MANE Select	NP_077310.1:p.Ala2Ser