Canonical Allele Identifier: CA2762548

Gene: TMEM44

Linked Data

• dbSNP Id: rs768376448
• ExAC: 3:194325126 C / T
• gnomAD v2: 3-194325126-C-T
• gnomAD v3: 3-194604397-C-T
• gnomAD v4: 3-194604397-C-T
• COSMIC: COSM1421792 ; COSM1421793
• MyVariant Identifiers: chr3:g.194325126C>T (hg19) ; chr3:g.194604397C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604397C>T , CM000665.2:g.194604397C>T	GRCh38
NC_000003.11:g.194325126C>T , CM000665.1:g.194325126C>T	GRCh37
NC_000003.10:g.195806415C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1066G>A MANE Select	ENSP00000333355.6:p.Gly356Arg
ENST00000347147.8:c.1066G>A	ENSP00000333355.6:p.Gly356Arg
ENST00000381975.7:c.1062G>A	ENSP00000371402.3:p.Pro354=
ENST00000392432.6:c.1207G>A	ENSP00000376227.2:p.Gly403Arg
ENST00000419280.5:c.*362G>A	ENSP00000414077.1:n.*362G>A
ENST00000429560.1:c.258G>A	ENSP00000403053.1:p.Pro86=
ENST00000432352.5:c.340G>A	ENSP00000409963.1:p.Gly114Arg
ENST00000452358.5:c.565G>A	ENSP00000414333.1:p.Gly189Arg
ENST00000467284.1:n.112G>A
ENST00000473092.5:c.1066G>A	ENSP00000418674.1:p.Gly356Arg
ENST00000477651.5:n.830G>A
NM_001011655.2:c.1066G>A	NP_001011655.1:p.Gly356Arg
NM_001166305.1:c.1207G>A	NP_001159777.1:p.Gly403Arg
NM_001166306.1:c.1062G>A	NP_001159778.1:p.Pro354=
NM_138399.4:c.1066G>A	NP_612408.3:p.Gly356Arg
XM_005269371.3:c.1066G>A	XP_005269428.1:p.Gly356Arg
XM_011513318.1:c.1216G>A	XP_011511620.1:p.Gly406Arg
XM_011513319.1:c.1153G>A	XP_011511621.1:p.Gly385Arg
XM_011513320.1:c.1264G>A	XP_011511622.1:p.Gly422Arg
XM_011513321.1:c.1132G>A	XP_011511623.1:p.Gly378Arg
XM_011513322.1:c.1123G>A	XP_011511624.1:p.Gly375Arg
XM_011513323.1:c.961G>A	XP_011511625.1:p.Gly321Arg
XM_005269371.4:c.1066G>A	XP_005269428.1:p.Gly356Arg
XM_011513318.2:c.1216G>A	XP_011511620.1:p.Gly406Arg
XM_011513319.2:c.1153G>A	XP_011511621.1:p.Gly385Arg
XM_011513320.2:c.1264G>A	XP_011511622.1:p.Gly422Arg
XM_011513321.2:c.1132G>A	XP_011511623.1:p.Gly378Arg
XM_011513322.2:c.1123G>A	XP_011511624.1:p.Gly375Arg
XM_017007517.1:c.1075G>A	XP_016863006.1:p.Gly359Arg
XM_017007518.1:c.1075G>A	XP_016863007.1:p.Gly359Arg
NM_001011655.3:c.1066G>A MANE Select	NP_001011655.1:p.Gly356Arg
NM_001166305.2:c.1207G>A	NP_001159777.1:p.Gly403Arg
NM_001166306.2:c.1062G>A	NP_001159778.1:p.Pro354=
NM_138399.5:c.1066G>A	NP_612408.3:p.Gly356Arg