Canonical Allele Identifier: CA1346973744
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14141451T= , CM000665.2:g.14141451T= GRCh38
NC_000003.11:g.14182951T= , CM000665.1:g.14182951T= GRCh37
NC_000003.10:g.14157952T= NCBI36
NG_008975.1:g.21512T= , LRG_435:g.21512T=

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.*1031-142T= ENSP00000395617.1:n.*1031-142T=
ENST00000306077.5:c.1001-142T= MANE Select ENSP00000303992.5:n.1001-142T=
ENST00000306077.4:c.1001-142T= ENSP00000303992.4:n.1001-142T=
ENST00000601399.3:n.327+2154T=
ENST00000608606.1:c.236+2154T=
NM_024334.2:c.1001-142T= , LRG_435t1:c.1001-142T= NP_077310.1:n.1001-142T=
XM_011534109.1:c.896-142T= XP_011532411.1:n.896-142T=
XM_017007176.2:c.896-142T= XP_016862665.1:n.896-142T=
NM_024334.3:c.1001-142T= MANE Select NP_077310.1:n.1001-142T=