Canonical Allele Identifier: CA355824894

Gene: TMEM44

Linked Data

• MyVariant Identifiers: chr3:g.194325090G>C (hg19) ; chr3:g.194604361G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604361G>C , CM000665.2:g.194604361G>C	GRCh38
NC_000003.11:g.194325090G>C , CM000665.1:g.194325090G>C	GRCh37
NC_000003.10:g.195806379G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1102C>G MANE Select	ENSP00000333355.6:p.Pro368Ala
ENST00000347147.8:c.1102C>G	ENSP00000333355.6:p.Pro368Ala
ENST00000381975.7:c.1098C>G	ENSP00000371402.3:p.Leu366=
ENST00000392432.6:c.1243C>G	ENSP00000376227.2:p.Pro415Ala
ENST00000419280.5:c.*398C>G	ENSP00000414077.1:n.*398C>G
ENST00000429560.1:c.294C>G	ENSP00000403053.1:p.Leu98=
ENST00000432352.5:c.376C>G	ENSP00000409963.1:p.Pro126Ala
ENST00000452358.5:c.601C>G	ENSP00000414333.1:p.Pro201Ala
ENST00000467284.1:n.148C>G
ENST00000473092.5:c.1102C>G	ENSP00000418674.1:p.Pro368Ala
ENST00000477651.5:n.866C>G
NM_001011655.2:c.1102C>G	NP_001011655.1:p.Pro368Ala
NM_001166305.1:c.1243C>G	NP_001159777.1:p.Pro415Ala
NM_001166306.1:c.1098C>G	NP_001159778.1:p.Leu366=
NM_138399.4:c.1102C>G	NP_612408.3:p.Pro368Ala
XM_005269371.3:c.1102C>G	XP_005269428.1:p.Pro368Ala
XM_011513318.1:c.1252C>G	XP_011511620.1:p.Pro418Ala
XM_011513319.1:c.1189C>G	XP_011511621.1:p.Pro397Ala
XM_011513320.1:c.1300C>G	XP_011511622.1:p.Pro434Ala
XM_011513321.1:c.1168C>G	XP_011511623.1:p.Pro390Ala
XM_011513322.1:c.1159C>G	XP_011511624.1:p.Pro387Ala
XM_011513323.1:c.997C>G	XP_011511625.1:p.Pro333Ala
XM_005269371.4:c.1102C>G	XP_005269428.1:p.Pro368Ala
XM_011513318.2:c.1252C>G	XP_011511620.1:p.Pro418Ala
XM_011513319.2:c.1189C>G	XP_011511621.1:p.Pro397Ala
XM_011513320.2:c.1300C>G	XP_011511622.1:p.Pro434Ala
XM_011513321.2:c.1168C>G	XP_011511623.1:p.Pro390Ala
XM_011513322.2:c.1159C>G	XP_011511624.1:p.Pro387Ala
XM_017007517.1:c.1111C>G	XP_016863006.1:p.Pro371Ala
XM_017007518.1:c.1111C>G	XP_016863007.1:p.Pro371Ala
NM_001011655.3:c.1102C>G MANE Select	NP_001011655.1:p.Pro368Ala
NM_001166305.2:c.1243C>G	NP_001159777.1:p.Pro415Ala
NM_001166306.2:c.1098C>G	NP_001159778.1:p.Leu366=
NM_138399.5:c.1102C>G	NP_612408.3:p.Pro368Ala