Canonical Allele Identifier: CA2577516633
Gene: TMEM43 HGNC NCBI

Linked Data

gnomAD v4: 3-14141538-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14141538T>G , CM000665.2:g.14141538T>G GRCh38
NC_000003.11:g.14183038T>G , CM000665.1:g.14183038T>G GRCh37
NC_000003.10:g.14158039T>G NCBI36
NG_008975.1:g.21599T>G , LRG_435:g.21599T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*1031-55T>G ENSP00000395617.1:n.*1031-55T>G
ENST00000306077.5:c.1001-55T>G MANE Select ENSP00000303992.5:n.1001-55T>G
ENST00000306077.4:c.1001-55T>G ENSP00000303992.4:n.1001-55T>G
ENST00000601399.3:n.327+2241T>G
ENST00000608606.1:c.236+2241T>G
NM_024334.2:c.1001-55T>G , LRG_435t1:c.1001-55T>G NP_077310.1:n.1001-55T>G
XM_011534109.1:c.896-55T>G XP_011532411.1:n.896-55T>G
XM_017007176.2:c.896-55T>G XP_016862665.1:n.896-55T>G
NM_024334.3:c.1001-55T>G MANE Select NP_077310.1:n.1001-55T>G