Canonical Allele Identifier: CA2669137989

Gene: TMEM44

Linked Data

• gnomAD v4: 3-194604597-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604597_194604598insGG , CM000665.2:g.194604597_194604598insGG	GRCh38
NC_000003.11:g.194325326_194325327insGG , CM000665.1:g.194325326_194325327insGG	GRCh37
NC_000003.10:g.195806615_195806616insGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1018-153_1018-152insCC MANE Select	ENSP00000333355.6:n.1018-153_1018-152insCC
ENST00000347147.8:c.1018-153_1018-152insCC	ENSP00000333355.6:n.1018-153_1018-152insCC
ENST00000381975.7:c.1018-157_1018-156insCC	ENSP00000371402.3:n.1018-157_1018-156insCC
ENST00000392432.6:c.1159-153_1159-152insCC	ENSP00000376227.2:n.1159-153_1159-152insCC
ENST00000419280.5:c.*314-153_*314-152insCC	ENSP00000414077.1:n.*314-153_*314-152insCC
ENST00000429560.1:c.214-157_214-156insCC	ENSP00000403053.1:n.214-157_214-156insCC
ENST00000432352.5:c.292-153_292-152insCC	ENSP00000409963.1:n.292-153_292-152insCC
ENST00000452358.5:c.517-153_517-152insCC	ENSP00000414333.1:n.517-153_517-152insCC
ENST00000467284.1:n.64-153_64-152insCC
ENST00000473092.5:c.1018-153_1018-152insCC	ENSP00000418674.1:n.1018-153_1018-152insCC
ENST00000477651.5:n.782-153_782-152insCC
NM_001011655.2:c.1018-153_1018-152insCC	NP_001011655.1:n.1018-153_1018-152insCC
NM_001166305.1:c.1159-153_1159-152insCC	NP_001159777.1:n.1159-153_1159-152insCC
NM_001166306.1:c.1018-157_1018-156insCC	NP_001159778.1:n.1018-157_1018-156insCC
NM_138399.4:c.1018-153_1018-152insCC	NP_612408.3:n.1018-153_1018-152insCC
XM_005269371.3:c.1018-153_1018-152insCC	XP_005269428.1:n.1018-153_1018-152insCC
XM_011513318.1:c.1168-153_1168-152insCC	XP_011511620.1:n.1168-153_1168-152insCC
XM_011513319.1:c.1105-153_1105-152insCC	XP_011511621.1:n.1105-153_1105-152insCC
XM_011513320.1:c.1216-153_1216-152insCC	XP_011511622.1:n.1216-153_1216-152insCC
XM_011513321.1:c.1084-153_1084-152insCC	XP_011511623.1:n.1084-153_1084-152insCC
XM_011513322.1:c.1075-153_1075-152insCC	XP_011511624.1:n.1075-153_1075-152insCC
XM_011513323.1:c.913-153_913-152insCC	XP_011511625.1:n.913-153_913-152insCC
XM_005269371.4:c.1018-153_1018-152insCC	XP_005269428.1:n.1018-153_1018-152insCC
XM_011513318.2:c.1168-153_1168-152insCC	XP_011511620.1:n.1168-153_1168-152insCC
XM_011513319.2:c.1105-153_1105-152insCC	XP_011511621.1:n.1105-153_1105-152insCC
XM_011513320.2:c.1216-153_1216-152insCC	XP_011511622.1:n.1216-153_1216-152insCC
XM_011513321.2:c.1084-153_1084-152insCC	XP_011511623.1:n.1084-153_1084-152insCC
XM_011513322.2:c.1075-153_1075-152insCC	XP_011511624.1:n.1075-153_1075-152insCC
XM_017007517.1:c.1027-153_1027-152insCC	XP_016863006.1:n.1027-153_1027-152insCC
XM_017007518.1:c.1027-153_1027-152insCC	XP_016863007.1:n.1027-153_1027-152insCC
NM_001011655.3:c.1018-153_1018-152insCC MANE Select	NP_001011655.1:n.1018-153_1018-152insCC
NM_001166305.2:c.1159-153_1159-152insCC	NP_001159777.1:n.1159-153_1159-152insCC
NM_001166306.2:c.1018-157_1018-156insCC	NP_001159778.1:n.1018-157_1018-156insCC
NM_138399.5:c.1018-153_1018-152insCC	NP_612408.3:n.1018-153_1018-152insCC