Canonical Allele Identifier: CA1346965696
Gene: TMEM43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14125191A= , CM000665.2:g.14125191A= GRCh38
NC_000003.11:g.14166691A= , CM000665.1:g.14166691A= GRCh37
NC_000003.10:g.14141692A= NCBI36
NG_008975.1:g.5252A= , LRG_435:g.5252A=

Transcript Alleles

HGVS Amino-acid change
ENST00000432444.2:c.-3A= ENSP00000395617.1:n.-3A=
ENST00000306077.5:c.-3A= MANE Select ENSP00000303992.5:n.-3A=
ENST00000306077.4:c.-3A= ENSP00000303992.4:n.-3A=
ENST00000432444.1:c.-3A= ENSP00000395617.1:n.-3A=
NM_024334.2:c.-3A= , LRG_435t1:c.-3A= NP_077310.1:n.-3A=
XM_017007176.2:c.-339A= XP_016862665.1:n.-339A=
NM_024334.3:c.-3A= MANE Select NP_077310.1:n.-3A=