Canonical Allele Identifier: CA2669137962

Gene: TMEM44

Linked Data

• gnomAD v4: 3-194604584-C-CCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604584_194604585insCAG , CM000665.2:g.194604584_194604585insCAG	GRCh38
NC_000003.11:g.194325313_194325314insCAG , CM000665.1:g.194325313_194325314insCAG	GRCh37
NC_000003.10:g.195806602_195806603insCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1018-140_1018-139insCTG MANE Select	ENSP00000333355.6:n.1018-140_1018-139insCTG
ENST00000347147.8:c.1018-140_1018-139insCTG	ENSP00000333355.6:n.1018-140_1018-139insCTG
ENST00000381975.7:c.1018-144_1018-143insCTG	ENSP00000371402.3:n.1018-144_1018-143insCTG
ENST00000392432.6:c.1159-140_1159-139insCTG	ENSP00000376227.2:n.1159-140_1159-139insCTG
ENST00000419280.5:c.*314-140_*314-139insCTG	ENSP00000414077.1:n.*314-140_*314-139insCTG
ENST00000429560.1:c.214-144_214-143insCTG	ENSP00000403053.1:n.214-144_214-143insCTG
ENST00000432352.5:c.292-140_292-139insCTG	ENSP00000409963.1:n.292-140_292-139insCTG
ENST00000452358.5:c.517-140_517-139insCTG	ENSP00000414333.1:n.517-140_517-139insCTG
ENST00000467284.1:n.64-140_64-139insCTG
ENST00000473092.5:c.1018-140_1018-139insCTG	ENSP00000418674.1:n.1018-140_1018-139insCTG
ENST00000477651.5:n.782-140_782-139insCTG
NM_001011655.2:c.1018-140_1018-139insCTG	NP_001011655.1:n.1018-140_1018-139insCTG
NM_001166305.1:c.1159-140_1159-139insCTG	NP_001159777.1:n.1159-140_1159-139insCTG
NM_001166306.1:c.1018-144_1018-143insCTG	NP_001159778.1:n.1018-144_1018-143insCTG
NM_138399.4:c.1018-140_1018-139insCTG	NP_612408.3:n.1018-140_1018-139insCTG
XM_005269371.3:c.1018-140_1018-139insCTG	XP_005269428.1:n.1018-140_1018-139insCTG
XM_011513318.1:c.1168-140_1168-139insCTG	XP_011511620.1:n.1168-140_1168-139insCTG
XM_011513319.1:c.1105-140_1105-139insCTG	XP_011511621.1:n.1105-140_1105-139insCTG
XM_011513320.1:c.1216-140_1216-139insCTG	XP_011511622.1:n.1216-140_1216-139insCTG
XM_011513321.1:c.1084-140_1084-139insCTG	XP_011511623.1:n.1084-140_1084-139insCTG
XM_011513322.1:c.1075-140_1075-139insCTG	XP_011511624.1:n.1075-140_1075-139insCTG
XM_011513323.1:c.913-140_913-139insCTG	XP_011511625.1:n.913-140_913-139insCTG
XM_005269371.4:c.1018-140_1018-139insCTG	XP_005269428.1:n.1018-140_1018-139insCTG
XM_011513318.2:c.1168-140_1168-139insCTG	XP_011511620.1:n.1168-140_1168-139insCTG
XM_011513319.2:c.1105-140_1105-139insCTG	XP_011511621.1:n.1105-140_1105-139insCTG
XM_011513320.2:c.1216-140_1216-139insCTG	XP_011511622.1:n.1216-140_1216-139insCTG
XM_011513321.2:c.1084-140_1084-139insCTG	XP_011511623.1:n.1084-140_1084-139insCTG
XM_011513322.2:c.1075-140_1075-139insCTG	XP_011511624.1:n.1075-140_1075-139insCTG
XM_017007517.1:c.1027-140_1027-139insCTG	XP_016863006.1:n.1027-140_1027-139insCTG
XM_017007518.1:c.1027-140_1027-139insCTG	XP_016863007.1:n.1027-140_1027-139insCTG
NM_001011655.3:c.1018-140_1018-139insCTG MANE Select	NP_001011655.1:n.1018-140_1018-139insCTG
NM_001166305.2:c.1159-140_1159-139insCTG	NP_001159777.1:n.1159-140_1159-139insCTG
NM_001166306.2:c.1018-144_1018-143insCTG	NP_001159778.1:n.1018-144_1018-143insCTG
NM_138399.5:c.1018-140_1018-139insCTG	NP_612408.3:n.1018-140_1018-139insCTG