Canonical Allele Identifier: CA355825035

Gene: TMEM44

Linked Data

• MyVariant Identifiers: chr3:g.194325144C>G (hg19) ; chr3:g.194604415C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604415C>G , CM000665.2:g.194604415C>G	GRCh38
NC_000003.11:g.194325144C>G , CM000665.1:g.194325144C>G	GRCh37
NC_000003.10:g.195806433C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1048G>C MANE Select	ENSP00000333355.6:p.Asp350His
ENST00000347147.8:c.1048G>C	ENSP00000333355.6:p.Asp350His
ENST00000381975.7:c.1044G>C	ENSP00000371402.3:p.Val348=
ENST00000392432.6:c.1189G>C	ENSP00000376227.2:p.Asp397His
ENST00000419280.5:c.*344G>C	ENSP00000414077.1:n.*344G>C
ENST00000429560.1:c.240G>C	ENSP00000403053.1:p.Val80=
ENST00000432352.5:c.322G>C	ENSP00000409963.1:p.Asp108His
ENST00000452358.5:c.547G>C	ENSP00000414333.1:p.Asp183His
ENST00000467284.1:n.94G>C
ENST00000473092.5:c.1048G>C	ENSP00000418674.1:p.Asp350His
ENST00000477651.5:n.812G>C
NM_001011655.2:c.1048G>C	NP_001011655.1:p.Asp350His
NM_001166305.1:c.1189G>C	NP_001159777.1:p.Asp397His
NM_001166306.1:c.1044G>C	NP_001159778.1:p.Val348=
NM_138399.4:c.1048G>C	NP_612408.3:p.Asp350His
XM_005269371.3:c.1048G>C	XP_005269428.1:p.Asp350His
XM_011513318.1:c.1198G>C	XP_011511620.1:p.Asp400His
XM_011513319.1:c.1135G>C	XP_011511621.1:p.Asp379His
XM_011513320.1:c.1246G>C	XP_011511622.1:p.Asp416His
XM_011513321.1:c.1114G>C	XP_011511623.1:p.Asp372His
XM_011513322.1:c.1105G>C	XP_011511624.1:p.Asp369His
XM_011513323.1:c.943G>C	XP_011511625.1:p.Asp315His
XM_005269371.4:c.1048G>C	XP_005269428.1:p.Asp350His
XM_011513318.2:c.1198G>C	XP_011511620.1:p.Asp400His
XM_011513319.2:c.1135G>C	XP_011511621.1:p.Asp379His
XM_011513320.2:c.1246G>C	XP_011511622.1:p.Asp416His
XM_011513321.2:c.1114G>C	XP_011511623.1:p.Asp372His
XM_011513322.2:c.1105G>C	XP_011511624.1:p.Asp369His
XM_017007517.1:c.1057G>C	XP_016863006.1:p.Asp353His
XM_017007518.1:c.1057G>C	XP_016863007.1:p.Asp353His
NM_001011655.3:c.1048G>C MANE Select	NP_001011655.1:p.Asp350His
NM_001166305.2:c.1189G>C	NP_001159777.1:p.Asp397His
NM_001166306.2:c.1044G>C	NP_001159778.1:p.Val348=
NM_138399.5:c.1048G>C	NP_612408.3:p.Asp350His