Canonical Allele Identifier: CA1346973775
Gene: TMEM43 HGNC NCBI

Linked Data

dbSNP Id: rs1695245484

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14141525del , CM000665.2:g.14141525del GRCh38
NC_000003.11:g.14183025del , CM000665.1:g.14183025del GRCh37
NC_000003.10:g.14158026del NCBI36
NG_008975.1:g.21586del , LRG_435:g.21586del

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*1031-68del ENSP00000395617.1:n.*1031-68del
ENST00000306077.5:c.1001-68del MANE Select ENSP00000303992.5:n.1001-68del
ENST00000306077.4:c.1001-68del ENSP00000303992.4:n.1001-68del
ENST00000601399.3:n.327+2228del
ENST00000608606.1:c.236+2228del
NM_024334.2:c.1001-68del , LRG_435t1:c.1001-68del NP_077310.1:n.1001-68del
XM_011534109.1:c.896-68del XP_011532411.1:n.896-68del
XM_017007176.2:c.896-68del XP_016862665.1:n.896-68del
NM_024334.3:c.1001-68del MANE Select NP_077310.1:n.1001-68del