Canonical Allele Identifier: CA1430709559

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604618_194604620delinsCCT , CM000665.2:g.194604618_194604620delinsCCT	GRCh38
NC_000003.11:g.194325347_194325349delinsCCT , CM000665.1:g.194325347_194325349delinsCCT	GRCh37
NC_000003.10:g.195806636_195806638delinsCCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1018-175_1018-173delinsAGG MANE Select	ENSP00000333355.6:n.1018-175_1018-173delinsAGG
ENST00000347147.8:c.1018-175_1018-173delinsAGG	ENSP00000333355.6:n.1018-175_1018-173delinsAGG
ENST00000381975.7:c.1018-179_1018-177delinsAGG	ENSP00000371402.3:n.1018-179_1018-177delinsAGG
ENST00000392432.6:c.1159-175_1159-173delinsAGG	ENSP00000376227.2:n.1159-175_1159-173delinsAGG
ENST00000419280.5:c.*314-175_*314-173delinsAGG	ENSP00000414077.1:n.*314-175_*314-173delinsAGG
ENST00000429560.1:c.214-179_214-177delinsAGG	ENSP00000403053.1:n.214-179_214-177delinsAGG
ENST00000432352.5:c.292-175_292-173delinsAGG	ENSP00000409963.1:n.292-175_292-173delinsAGG
ENST00000452358.5:c.517-175_517-173delinsAGG	ENSP00000414333.1:n.517-175_517-173delinsAGG
ENST00000467284.1:n.64-175_64-173delinsAGG
ENST00000473092.5:c.1018-175_1018-173delinsAGG	ENSP00000418674.1:n.1018-175_1018-173delinsAGG
ENST00000477651.5:n.782-175_782-173delinsAGG
NM_001011655.2:c.1018-175_1018-173delinsAGG	NP_001011655.1:n.1018-175_1018-173delinsAGG
NM_001166305.1:c.1159-175_1159-173delinsAGG	NP_001159777.1:n.1159-175_1159-173delinsAGG
NM_001166306.1:c.1018-179_1018-177delinsAGG	NP_001159778.1:n.1018-179_1018-177delinsAGG
NM_138399.4:c.1018-175_1018-173delinsAGG	NP_612408.3:n.1018-175_1018-173delinsAGG
XM_005269371.3:c.1018-175_1018-173delinsAGG	XP_005269428.1:n.1018-175_1018-173delinsAGG
XM_011513318.1:c.1168-175_1168-173delinsAGG	XP_011511620.1:n.1168-175_1168-173delinsAGG
XM_011513319.1:c.1105-175_1105-173delinsAGG	XP_011511621.1:n.1105-175_1105-173delinsAGG
XM_011513320.1:c.1216-175_1216-173delinsAGG	XP_011511622.1:n.1216-175_1216-173delinsAGG
XM_011513321.1:c.1084-175_1084-173delinsAGG	XP_011511623.1:n.1084-175_1084-173delinsAGG
XM_011513322.1:c.1075-175_1075-173delinsAGG	XP_011511624.1:n.1075-175_1075-173delinsAGG
XM_011513323.1:c.913-175_913-173delinsAGG	XP_011511625.1:n.913-175_913-173delinsAGG
XM_005269371.4:c.1018-175_1018-173delinsAGG	XP_005269428.1:n.1018-175_1018-173delinsAGG
XM_011513318.2:c.1168-175_1168-173delinsAGG	XP_011511620.1:n.1168-175_1168-173delinsAGG
XM_011513319.2:c.1105-175_1105-173delinsAGG	XP_011511621.1:n.1105-175_1105-173delinsAGG
XM_011513320.2:c.1216-175_1216-173delinsAGG	XP_011511622.1:n.1216-175_1216-173delinsAGG
XM_011513321.2:c.1084-175_1084-173delinsAGG	XP_011511623.1:n.1084-175_1084-173delinsAGG
XM_011513322.2:c.1075-175_1075-173delinsAGG	XP_011511624.1:n.1075-175_1075-173delinsAGG
XM_017007517.1:c.1027-175_1027-173delinsAGG	XP_016863006.1:n.1027-175_1027-173delinsAGG
XM_017007518.1:c.1027-175_1027-173delinsAGG	XP_016863007.1:n.1027-175_1027-173delinsAGG
NM_001011655.3:c.1018-175_1018-173delinsAGG MANE Select	NP_001011655.1:n.1018-175_1018-173delinsAGG
NM_001166305.2:c.1159-175_1159-173delinsAGG	NP_001159777.1:n.1159-175_1159-173delinsAGG
NM_001166306.2:c.1018-179_1018-177delinsAGG	NP_001159778.1:n.1018-179_1018-177delinsAGG
NM_138399.5:c.1018-175_1018-173delinsAGG	NP_612408.3:n.1018-175_1018-173delinsAGG