Canonical Allele Identifier: CA1346973781

Gene: TMEM43

Linked Data

• dbSNP Id: rs1695245614

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14141541del , CM000665.2:g.14141541del	GRCh38
NC_000003.11:g.14183041del , CM000665.1:g.14183041del	GRCh37
NC_000003.10:g.14158042del	NCBI36
NG_008975.1:g.21602del , LRG_435:g.21602del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432444.2:c.*1031-52del	ENSP00000395617.1:n.*1031-52del
ENST00000306077.5:c.1001-52del MANE Select	ENSP00000303992.5:n.1001-52del
ENST00000306077.4:c.1001-52del	ENSP00000303992.4:n.1001-52del
ENST00000601399.3:n.327+2244del
ENST00000608606.1:c.236+2244del
NM_024334.2:c.1001-52del , LRG_435t1:c.1001-52del	NP_077310.1:n.1001-52del
XM_011534109.1:c.896-52del	XP_011532411.1:n.896-52del
XM_017007176.2:c.896-52del	XP_016862665.1:n.896-52del
NM_024334.3:c.1001-52del MANE Select	NP_077310.1:n.1001-52del