Canonical Allele Identifier: CA1430709441

Gene: TMEM44

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.194604460_194604461delinsAG , CM000665.2:g.194604460_194604461delinsAG	GRCh38
NC_000003.11:g.194325189_194325190delinsAG , CM000665.1:g.194325189_194325190delinsAG	GRCh37
NC_000003.10:g.195806478_195806479delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347147.9:c.1018-16_1018-15delinsCT MANE Select	ENSP00000333355.6:n.1018-16_1018-15delinsCT
ENST00000347147.8:c.1018-16_1018-15delinsCT	ENSP00000333355.6:n.1018-16_1018-15delinsCT
ENST00000381975.7:c.1018-20_1018-19delinsCT	ENSP00000371402.3:n.1018-20_1018-19delinsCT
ENST00000392432.6:c.1159-16_1159-15delinsCT	ENSP00000376227.2:n.1159-16_1159-15delinsCT
ENST00000419280.5:c.*314-16_*314-15delinsCT	ENSP00000414077.1:n.*314-16_*314-15delinsCT
ENST00000429560.1:c.214-20_214-19delinsCT	ENSP00000403053.1:n.214-20_214-19delinsCT
ENST00000432352.5:c.292-16_292-15delinsCT	ENSP00000409963.1:n.292-16_292-15delinsCT
ENST00000452358.5:c.517-16_517-15delinsCT	ENSP00000414333.1:n.517-16_517-15delinsCT
ENST00000467284.1:n.64-16_64-15delinsCT
ENST00000473092.5:c.1018-16_1018-15delinsCT	ENSP00000418674.1:n.1018-16_1018-15delinsCT
ENST00000477651.5:n.782-16_782-15delinsCT
NM_001011655.2:c.1018-16_1018-15delinsCT	NP_001011655.1:n.1018-16_1018-15delinsCT
NM_001166305.1:c.1159-16_1159-15delinsCT	NP_001159777.1:n.1159-16_1159-15delinsCT
NM_001166306.1:c.1018-20_1018-19delinsCT	NP_001159778.1:n.1018-20_1018-19delinsCT
NM_138399.4:c.1018-16_1018-15delinsCT	NP_612408.3:n.1018-16_1018-15delinsCT
XM_005269371.3:c.1018-16_1018-15delinsCT	XP_005269428.1:n.1018-16_1018-15delinsCT
XM_011513318.1:c.1168-16_1168-15delinsCT	XP_011511620.1:n.1168-16_1168-15delinsCT
XM_011513319.1:c.1105-16_1105-15delinsCT	XP_011511621.1:n.1105-16_1105-15delinsCT
XM_011513320.1:c.1216-16_1216-15delinsCT	XP_011511622.1:n.1216-16_1216-15delinsCT
XM_011513321.1:c.1084-16_1084-15delinsCT	XP_011511623.1:n.1084-16_1084-15delinsCT
XM_011513322.1:c.1075-16_1075-15delinsCT	XP_011511624.1:n.1075-16_1075-15delinsCT
XM_011513323.1:c.913-16_913-15delinsCT	XP_011511625.1:n.913-16_913-15delinsCT
XM_005269371.4:c.1018-16_1018-15delinsCT	XP_005269428.1:n.1018-16_1018-15delinsCT
XM_011513318.2:c.1168-16_1168-15delinsCT	XP_011511620.1:n.1168-16_1168-15delinsCT
XM_011513319.2:c.1105-16_1105-15delinsCT	XP_011511621.1:n.1105-16_1105-15delinsCT
XM_011513320.2:c.1216-16_1216-15delinsCT	XP_011511622.1:n.1216-16_1216-15delinsCT
XM_011513321.2:c.1084-16_1084-15delinsCT	XP_011511623.1:n.1084-16_1084-15delinsCT
XM_011513322.2:c.1075-16_1075-15delinsCT	XP_011511624.1:n.1075-16_1075-15delinsCT
XM_017007517.1:c.1027-16_1027-15delinsCT	XP_016863006.1:n.1027-16_1027-15delinsCT
XM_017007518.1:c.1027-16_1027-15delinsCT	XP_016863007.1:n.1027-16_1027-15delinsCT
NM_001011655.3:c.1018-16_1018-15delinsCT MANE Select	NP_001011655.1:n.1018-16_1018-15delinsCT
NM_001166305.2:c.1159-16_1159-15delinsCT	NP_001159777.1:n.1159-16_1159-15delinsCT
NM_001166306.2:c.1018-20_1018-19delinsCT	NP_001159778.1:n.1018-20_1018-19delinsCT
NM_138399.5:c.1018-16_1018-15delinsCT	NP_612408.3:n.1018-16_1018-15delinsCT