Canonical Allele Identifier: CA899785750

Gene: TMEM43

Linked Data

• dbSNP Id: rs1266777429
• gnomAD v3: 3-14141526-G-C
• gnomAD v4: 3-14141526-G-C
• MyVariant Identifiers: chr3:g.14183026G>C (hg19) ; chr3:g.14141526G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14141526G>C , CM000665.2:g.14141526G>C	GRCh38
NC_000003.11:g.14183026G>C , CM000665.1:g.14183026G>C	GRCh37
NC_000003.10:g.14158027G>C	NCBI36
NG_008975.1:g.21587G>C , LRG_435:g.21587G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000432444.2:c.*1031-67G>C	ENSP00000395617.1:n.*1031-67G>C
ENST00000306077.5:c.1001-67G>C MANE Select	ENSP00000303992.5:n.1001-67G>C
ENST00000306077.4:c.1001-67G>C	ENSP00000303992.4:n.1001-67G>C
ENST00000601399.3:n.327+2229G>C
ENST00000608606.1:c.236+2229G>C
NM_024334.2:c.1001-67G>C , LRG_435t1:c.1001-67G>C	NP_077310.1:n.1001-67G>C
XM_011534109.1:c.896-67G>C	XP_011532411.1:n.896-67G>C
XM_017007176.2:c.896-67G>C	XP_016862665.1:n.896-67G>C
NM_024334.3:c.1001-67G>C MANE Select	NP_077310.1:n.1001-67G>C