Canonical Allele Identifier: CA355825002

Gene: TMEM44

Linked Data

• MyVariant Identifiers: chr3:g.194325131C>T (hg19) ; chr3:g.194604402C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604402C>T , CM000665.2:g.194604402C>T	GRCh38
NC_000003.11:g.194325131C>T , CM000665.1:g.194325131C>T	GRCh37
NC_000003.10:g.195806420C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1061G>A MANE Select	ENSP00000333355.6:p.Ser354Asn
ENST00000347147.8:c.1061G>A	ENSP00000333355.6:p.Ser354Asn
ENST00000381975.7:c.1057G>A	ENSP00000371402.3:p.Ala353Thr
ENST00000392432.6:c.1202G>A	ENSP00000376227.2:p.Ser401Asn
ENST00000419280.5:c.*357G>A	ENSP00000414077.1:n.*357G>A
ENST00000429560.1:c.253G>A	ENSP00000403053.1:p.Ala85Thr
ENST00000432352.5:c.335G>A	ENSP00000409963.1:p.Ser112Asn
ENST00000452358.5:c.560G>A	ENSP00000414333.1:p.Ser187Asn
ENST00000467284.1:n.107G>A
ENST00000473092.5:c.1061G>A	ENSP00000418674.1:p.Ser354Asn
ENST00000477651.5:n.825G>A
NM_001011655.2:c.1061G>A	NP_001011655.1:p.Ser354Asn
NM_001166305.1:c.1202G>A	NP_001159777.1:p.Ser401Asn
NM_001166306.1:c.1057G>A	NP_001159778.1:p.Ala353Thr
NM_138399.4:c.1061G>A	NP_612408.3:p.Ser354Asn
XM_005269371.3:c.1061G>A	XP_005269428.1:p.Ser354Asn
XM_011513318.1:c.1211G>A	XP_011511620.1:p.Ser404Asn
XM_011513319.1:c.1148G>A	XP_011511621.1:p.Ser383Asn
XM_011513320.1:c.1259G>A	XP_011511622.1:p.Ser420Asn
XM_011513321.1:c.1127G>A	XP_011511623.1:p.Ser376Asn
XM_011513322.1:c.1118G>A	XP_011511624.1:p.Ser373Asn
XM_011513323.1:c.956G>A	XP_011511625.1:p.Ser319Asn
XM_005269371.4:c.1061G>A	XP_005269428.1:p.Ser354Asn
XM_011513318.2:c.1211G>A	XP_011511620.1:p.Ser404Asn
XM_011513319.2:c.1148G>A	XP_011511621.1:p.Ser383Asn
XM_011513320.2:c.1259G>A	XP_011511622.1:p.Ser420Asn
XM_011513321.2:c.1127G>A	XP_011511623.1:p.Ser376Asn
XM_011513322.2:c.1118G>A	XP_011511624.1:p.Ser373Asn
XM_017007517.1:c.1070G>A	XP_016863006.1:p.Ser357Asn
XM_017007518.1:c.1070G>A	XP_016863007.1:p.Ser357Asn
NM_001011655.3:c.1061G>A MANE Select	NP_001011655.1:p.Ser354Asn
NM_001166305.2:c.1202G>A	NP_001159777.1:p.Ser401Asn
NM_001166306.2:c.1057G>A	NP_001159778.1:p.Ala353Thr
NM_138399.5:c.1061G>A	NP_612408.3:p.Ser354Asn