Canonical Allele Identifier: CA432550638

Gene: TMEM43

Linked Data

• MyVariant Identifiers: chr3:g.14166702G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14125202G>T , CM000665.2:g.14125202G>T	GRCh38
NC_000003.11:g.14166702G>T , CM000665.1:g.14166702G>T	GRCh37
NC_000003.10:g.14141703G>T	NCBI36
NG_008975.1:g.5263G>T , LRG_435:g.5263G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000432444.2:c.9G>T	ENSP00000395617.1:p.Ala3=
ENST00000306077.5:c.9G>T MANE Select	ENSP00000303992.5:p.Ala3=
ENST00000306077.4:c.9G>T	ENSP00000303992.4:p.Ala3=
ENST00000432444.1:c.9G>T	ENSP00000395617.1:p.Ala3=
NM_024334.2:c.9G>T , LRG_435t1:c.9G>T	NP_077310.1:p.Ala3=
XM_017007176.2:c.-328G>T	XP_016862665.1:n.-328G>T
NM_024334.3:c.9G>T MANE Select	NP_077310.1:p.Ala3=