Canonical Allele Identifier: CA355824935

Gene: TMEM44

Linked Data

• dbSNP Id: rs1577175655
• MyVariant Identifiers: chr3:g.194325106G>C (hg19) ; chr3:g.194604377G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604377G>C , CM000665.2:g.194604377G>C	GRCh38
NC_000003.11:g.194325106G>C , CM000665.1:g.194325106G>C	GRCh37
NC_000003.10:g.195806395G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1086C>G MANE Select	ENSP00000333355.6:p.Asp362Glu
ENST00000347147.8:c.1086C>G	ENSP00000333355.6:p.Asp362Glu
ENST00000381975.7:c.1082C>G	ENSP00000371402.3:p.Thr361Ser
ENST00000392432.6:c.1227C>G	ENSP00000376227.2:p.Asp409Glu
ENST00000419280.5:c.*382C>G	ENSP00000414077.1:n.*382C>G
ENST00000429560.1:c.278C>G	ENSP00000403053.1:p.Thr93Ser
ENST00000432352.5:c.360C>G	ENSP00000409963.1:p.Asp120Glu
ENST00000452358.5:c.585C>G	ENSP00000414333.1:p.Asp195Glu
ENST00000467284.1:n.132C>G
ENST00000473092.5:c.1086C>G	ENSP00000418674.1:p.Asp362Glu
ENST00000477651.5:n.850C>G
NM_001011655.2:c.1086C>G	NP_001011655.1:p.Asp362Glu
NM_001166305.1:c.1227C>G	NP_001159777.1:p.Asp409Glu
NM_001166306.1:c.1082C>G	NP_001159778.1:p.Thr361Ser
NM_138399.4:c.1086C>G	NP_612408.3:p.Asp362Glu
XM_005269371.3:c.1086C>G	XP_005269428.1:p.Asp362Glu
XM_011513318.1:c.1236C>G	XP_011511620.1:p.Asp412Glu
XM_011513319.1:c.1173C>G	XP_011511621.1:p.Asp391Glu
XM_011513320.1:c.1284C>G	XP_011511622.1:p.Asp428Glu
XM_011513321.1:c.1152C>G	XP_011511623.1:p.Asp384Glu
XM_011513322.1:c.1143C>G	XP_011511624.1:p.Asp381Glu
XM_011513323.1:c.981C>G	XP_011511625.1:p.Asp327Glu
XM_005269371.4:c.1086C>G	XP_005269428.1:p.Asp362Glu
XM_011513318.2:c.1236C>G	XP_011511620.1:p.Asp412Glu
XM_011513319.2:c.1173C>G	XP_011511621.1:p.Asp391Glu
XM_011513320.2:c.1284C>G	XP_011511622.1:p.Asp428Glu
XM_011513321.2:c.1152C>G	XP_011511623.1:p.Asp384Glu
XM_011513322.2:c.1143C>G	XP_011511624.1:p.Asp381Glu
XM_017007517.1:c.1095C>G	XP_016863006.1:p.Asp365Glu
XM_017007518.1:c.1095C>G	XP_016863007.1:p.Asp365Glu
NM_001011655.3:c.1086C>G MANE Select	NP_001011655.1:p.Asp362Glu
NM_001166305.2:c.1227C>G	NP_001159777.1:p.Asp409Glu
NM_001166306.2:c.1082C>G	NP_001159778.1:p.Thr361Ser
NM_138399.5:c.1086C>G	NP_612408.3:p.Asp362Glu