Canonical Allele Identifier: CA69728920
Gene: TMEM43 HGNC NCBI

Linked Data

dbSNP Id: rs968206484
gnomAD v2: 3-14172223-G-A
gnomAD v3: 3-14130723-G-A
gnomAD v4: 3-14130723-G-A
MyVariant Identifiers: chr3:g.14172223G>A (hg19) chr3:g.14130723G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.14130723G>A , CM000665.2:g.14130723G>A GRCh38
NC_000003.11:g.14172223G>A , CM000665.1:g.14172223G>A GRCh37
NC_000003.10:g.14147224G>A NCBI36
NG_008975.1:g.10784G>A , LRG_435:g.10784G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000432444.2:c.*193-99G>A ENSP00000395617.1:n.*193-99G>A
ENST00000306077.5:c.163-99G>A MANE Select ENSP00000303992.5:n.163-99G>A
ENST00000306077.4:c.163-99G>A ENSP00000303992.4:n.163-99G>A
ENST00000432444.1:c.*193-99G>A ENSP00000395617.1:n.*193-99G>A
NM_024334.2:c.163-99G>A , LRG_435t1:c.163-99G>A NP_077310.1:n.163-99G>A
XM_011534109.1:c.58-99G>A XP_011532411.1:n.58-99G>A
XM_017007176.2:c.58-99G>A XP_016862665.1:n.58-99G>A
NM_024334.3:c.163-99G>A MANE Select NP_077310.1:n.163-99G>A
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