Canonical Allele Identifier: CA355825065

Gene: TMEM44

Linked Data

• dbSNP Id: rs1372833822
• gnomAD v2: 3-194325155-C-T
• gnomAD v3: 3-194604426-C-T
• gnomAD v4: 3-194604426-C-T
• MyVariant Identifiers: chr3:g.194325155C>T (hg19) ; chr3:g.194604426C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604426C>T , CM000665.2:g.194604426C>T	GRCh38
NC_000003.11:g.194325155C>T , CM000665.1:g.194325155C>T	GRCh37
NC_000003.10:g.195806444C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1037G>A MANE Select	ENSP00000333355.6:p.Arg346Lys
ENST00000347147.8:c.1037G>A	ENSP00000333355.6:p.Arg346Lys
ENST00000381975.7:c.1033G>A	ENSP00000371402.3:p.Gly345Ser
ENST00000392432.6:c.1178G>A	ENSP00000376227.2:p.Arg393Lys
ENST00000419280.5:c.*333G>A	ENSP00000414077.1:n.*333G>A
ENST00000429560.1:c.229G>A	ENSP00000403053.1:p.Gly77Ser
ENST00000432352.5:c.311G>A	ENSP00000409963.1:p.Arg104Lys
ENST00000452358.5:c.536G>A	ENSP00000414333.1:p.Arg179Lys
ENST00000467284.1:n.83G>A
ENST00000473092.5:c.1037G>A	ENSP00000418674.1:p.Arg346Lys
ENST00000477651.5:n.801G>A
NM_001011655.2:c.1037G>A	NP_001011655.1:p.Arg346Lys
NM_001166305.1:c.1178G>A	NP_001159777.1:p.Arg393Lys
NM_001166306.1:c.1033G>A	NP_001159778.1:p.Gly345Ser
NM_138399.4:c.1037G>A	NP_612408.3:p.Arg346Lys
XM_005269371.3:c.1037G>A	XP_005269428.1:p.Arg346Lys
XM_011513318.1:c.1187G>A	XP_011511620.1:p.Arg396Lys
XM_011513319.1:c.1124G>A	XP_011511621.1:p.Arg375Lys
XM_011513320.1:c.1235G>A	XP_011511622.1:p.Arg412Lys
XM_011513321.1:c.1103G>A	XP_011511623.1:p.Arg368Lys
XM_011513322.1:c.1094G>A	XP_011511624.1:p.Arg365Lys
XM_011513323.1:c.932G>A	XP_011511625.1:p.Arg311Lys
XM_005269371.4:c.1037G>A	XP_005269428.1:p.Arg346Lys
XM_011513318.2:c.1187G>A	XP_011511620.1:p.Arg396Lys
XM_011513319.2:c.1124G>A	XP_011511621.1:p.Arg375Lys
XM_011513320.2:c.1235G>A	XP_011511622.1:p.Arg412Lys
XM_011513321.2:c.1103G>A	XP_011511623.1:p.Arg368Lys
XM_011513322.2:c.1094G>A	XP_011511624.1:p.Arg365Lys
XM_017007517.1:c.1046G>A	XP_016863006.1:p.Arg349Lys
XM_017007518.1:c.1046G>A	XP_016863007.1:p.Arg349Lys
NM_001011655.3:c.1037G>A MANE Select	NP_001011655.1:p.Arg346Lys
NM_001166305.2:c.1178G>A	NP_001159777.1:p.Arg393Lys
NM_001166306.2:c.1033G>A	NP_001159778.1:p.Gly345Ser
NM_138399.5:c.1037G>A	NP_612408.3:p.Arg346Lys