Canonical Allele Identifier: CA351536406
Gene: TMEM43 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*1063A>C ENSP00000395617.1:n.*1063A>C
ENST00000306077.5:c.1033A>C MANE Select ENSP00000303992.5:p.Asn345His
ENST00000306077.4:c.1033A>C ENSP00000303992.4:p.Asn345His
ENST00000601399.3:n.327+2328A>C
ENST00000608606.1:c.236+2328A>C
NM_024334.2:c.1033A>C , LRG_435t1:c.1033A>C NP_077310.1:p.Asn345His
XM_011534109.1:c.928A>C XP_011532411.1:p.Asn310His
XM_017007176.2:c.928A>C XP_016862665.1:p.Asn310His
NM_024334.3:c.1033A>C MANE Select NP_077310.1:p.Asn345His