Canonical Allele Identifier: CA432552859
Gene: TMEM43 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.14183121G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14141621G>A , CM000665.2:g.14141621G>A GRCh38
NC_000003.11:g.14183121G>A , CM000665.1:g.14183121G>A GRCh37
NC_000003.10:g.14158122G>A NCBI36
NG_008975.1:g.21682G>A , LRG_435:g.21682G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*1059G>A ENSP00000395617.1:n.*1059G>A
ENST00000306077.5:c.1029G>A MANE Select ENSP00000303992.5:p.Leu343=
ENST00000306077.4:c.1029G>A ENSP00000303992.4:p.Leu343=
ENST00000601399.3:n.327+2324G>A
ENST00000608606.1:c.236+2324G>A
NM_024334.2:c.1029G>A , LRG_435t1:c.1029G>A NP_077310.1:p.Leu343=
XM_011534109.1:c.924G>A XP_011532411.1:p.Leu308=
XM_017007176.2:c.924G>A XP_016862665.1:p.Leu308=
NM_024334.3:c.1029G>A MANE Select NP_077310.1:p.Leu343=