Canonical Allele Identifier: CA351536407
Gene: TMEM43 HGNC NCBI

Linked Data

dbSNP Id: rs1695247124
gnomAD v4: 3-14141625-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14141625A>G , CM000665.2:g.14141625A>G GRCh38
NC_000003.11:g.14183125A>G , CM000665.1:g.14183125A>G GRCh37
NC_000003.10:g.14158126A>G NCBI36
NG_008975.1:g.21686A>G , LRG_435:g.21686A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*1063A>G ENSP00000395617.1:n.*1063A>G
ENST00000306077.5:c.1033A>G MANE Select ENSP00000303992.5:p.Asn345Asp
ENST00000306077.4:c.1033A>G ENSP00000303992.4:p.Asn345Asp
ENST00000601399.3:n.327+2328A>G
ENST00000608606.1:c.236+2328A>G
NM_024334.2:c.1033A>G , LRG_435t1:c.1033A>G NP_077310.1:p.Asn345Asp
XM_011534109.1:c.928A>G XP_011532411.1:p.Asn310Asp
XM_017007176.2:c.928A>G XP_016862665.1:p.Asn310Asp
NM_024334.3:c.1033A>G MANE Select NP_077310.1:p.Asn345Asp