Canonical Allele Identifier: CA355824975

Gene: TMEM44

Linked Data

• MyVariant Identifiers: chr3:g.194325121A>G (hg19) ; chr3:g.194604392A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604392A>G , CM000665.2:g.194604392A>G	GRCh38
NC_000003.11:g.194325121A>G , CM000665.1:g.194325121A>G	GRCh37
NC_000003.10:g.195806410A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1071T>C MANE Select	ENSP00000333355.6:p.Asp357=
ENST00000347147.8:c.1071T>C	ENSP00000333355.6:p.Asp357=
ENST00000381975.7:c.1067T>C	ENSP00000371402.3:p.Met356Thr
ENST00000392432.6:c.1212T>C	ENSP00000376227.2:p.Asp404=
ENST00000419280.5:c.*367T>C	ENSP00000414077.1:n.*367T>C
ENST00000429560.1:c.263T>C	ENSP00000403053.1:p.Met88Thr
ENST00000432352.5:c.345T>C	ENSP00000409963.1:p.Asp115=
ENST00000452358.5:c.570T>C	ENSP00000414333.1:p.Asp190=
ENST00000467284.1:n.117T>C
ENST00000473092.5:c.1071T>C	ENSP00000418674.1:p.Asp357=
ENST00000477651.5:n.835T>C
NM_001011655.2:c.1071T>C	NP_001011655.1:p.Asp357=
NM_001166305.1:c.1212T>C	NP_001159777.1:p.Asp404=
NM_001166306.1:c.1067T>C	NP_001159778.1:p.Met356Thr
NM_138399.4:c.1071T>C	NP_612408.3:p.Asp357=
XM_005269371.3:c.1071T>C	XP_005269428.1:p.Asp357=
XM_011513318.1:c.1221T>C	XP_011511620.1:p.Asp407=
XM_011513319.1:c.1158T>C	XP_011511621.1:p.Asp386=
XM_011513320.1:c.1269T>C	XP_011511622.1:p.Asp423=
XM_011513321.1:c.1137T>C	XP_011511623.1:p.Asp379=
XM_011513322.1:c.1128T>C	XP_011511624.1:p.Asp376=
XM_011513323.1:c.966T>C	XP_011511625.1:p.Asp322=
XM_005269371.4:c.1071T>C	XP_005269428.1:p.Asp357=
XM_011513318.2:c.1221T>C	XP_011511620.1:p.Asp407=
XM_011513319.2:c.1158T>C	XP_011511621.1:p.Asp386=
XM_011513320.2:c.1269T>C	XP_011511622.1:p.Asp423=
XM_011513321.2:c.1137T>C	XP_011511623.1:p.Asp379=
XM_011513322.2:c.1128T>C	XP_011511624.1:p.Asp376=
XM_017007517.1:c.1080T>C	XP_016863006.1:p.Asp360=
XM_017007518.1:c.1080T>C	XP_016863007.1:p.Asp360=
NM_001011655.3:c.1071T>C MANE Select	NP_001011655.1:p.Asp357=
NM_001166305.2:c.1212T>C	NP_001159777.1:p.Asp404=
NM_001166306.2:c.1067T>C	NP_001159778.1:p.Met356Thr
NM_138399.5:c.1071T>C	NP_612408.3:p.Asp357=