Canonical Allele Identifier: CA355824943

Gene: TMEM44

Linked Data

• gnomAD v4: 3-194604380-C-A
• MyVariant Identifiers: chr3:g.194325109C>A (hg19) ; chr3:g.194604380C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604380C>A , CM000665.2:g.194604380C>A	GRCh38
NC_000003.11:g.194325109C>A , CM000665.1:g.194325109C>A	GRCh37
NC_000003.10:g.195806398C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1083G>T MANE Select	ENSP00000333355.6:p.Gln361His
ENST00000347147.8:c.1083G>T	ENSP00000333355.6:p.Gln361His
ENST00000381975.7:c.1079G>T	ENSP00000371402.3:p.Arg360Met
ENST00000392432.6:c.1224G>T	ENSP00000376227.2:p.Gln408His
ENST00000419280.5:c.*379G>T	ENSP00000414077.1:n.*379G>T
ENST00000429560.1:c.275G>T	ENSP00000403053.1:p.Arg92Met
ENST00000432352.5:c.357G>T	ENSP00000409963.1:p.Gln119His
ENST00000452358.5:c.582G>T	ENSP00000414333.1:p.Gln194His
ENST00000467284.1:n.129G>T
ENST00000473092.5:c.1083G>T	ENSP00000418674.1:p.Gln361His
ENST00000477651.5:n.847G>T
NM_001011655.2:c.1083G>T	NP_001011655.1:p.Gln361His
NM_001166305.1:c.1224G>T	NP_001159777.1:p.Gln408His
NM_001166306.1:c.1079G>T	NP_001159778.1:p.Arg360Met
NM_138399.4:c.1083G>T	NP_612408.3:p.Gln361His
XM_005269371.3:c.1083G>T	XP_005269428.1:p.Gln361His
XM_011513318.1:c.1233G>T	XP_011511620.1:p.Gln411His
XM_011513319.1:c.1170G>T	XP_011511621.1:p.Gln390His
XM_011513320.1:c.1281G>T	XP_011511622.1:p.Gln427His
XM_011513321.1:c.1149G>T	XP_011511623.1:p.Gln383His
XM_011513322.1:c.1140G>T	XP_011511624.1:p.Gln380His
XM_011513323.1:c.978G>T	XP_011511625.1:p.Gln326His
XM_005269371.4:c.1083G>T	XP_005269428.1:p.Gln361His
XM_011513318.2:c.1233G>T	XP_011511620.1:p.Gln411His
XM_011513319.2:c.1170G>T	XP_011511621.1:p.Gln390His
XM_011513320.2:c.1281G>T	XP_011511622.1:p.Gln427His
XM_011513321.2:c.1149G>T	XP_011511623.1:p.Gln383His
XM_011513322.2:c.1140G>T	XP_011511624.1:p.Gln380His
XM_017007517.1:c.1092G>T	XP_016863006.1:p.Gln364His
XM_017007518.1:c.1092G>T	XP_016863007.1:p.Gln364His
NM_001011655.3:c.1083G>T MANE Select	NP_001011655.1:p.Gln361His
NM_001166305.2:c.1224G>T	NP_001159777.1:p.Gln408His
NM_001166306.2:c.1079G>T	NP_001159778.1:p.Arg360Met
NM_138399.5:c.1083G>T	NP_612408.3:p.Gln361His