Canonical Allele Identifier: CA1058446277

Gene: TMEM175

Linked Data

• gnomAD v3: 4-945282-GT-G
• gnomAD v4: 4-945282-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.945285del , CM000666.2:g.945285del	GRCh38
NC_000004.11:g.939073del , CM000666.1:g.939073del	GRCh37
NC_000004.10:g.929073del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264771.9:c.-31-2424del MANE Select	ENSP00000264771.4:n.-31-2424del
ENST00000264771.8:c.-31-2424del	ENSP00000264771.4:n.-31-2424del
ENST00000438836.6:n.70-2424del
ENST00000452360.6:n.82-2424del
ENST00000504505.1:n.67-2424del
ENST00000504744.5:c.-31-2424del	ENSP00000423751.1:n.-31-2424del
ENST00000504850.1:n.55-714del
ENST00000505734.1:n.110-2424del
ENST00000507319.5:c.-31-2424del	ENSP00000424746.1:n.-31-2424del
ENST00000508204.5:c.-54-5136del	ENSP00000423669.1:n.-54-5136del
ENST00000509508.5:c.-54-5136del	ENSP00000421750.1:n.-54-5136del
ENST00000510493.5:c.-93-2831del	ENSP00000424208.1:n.-93-2831del
ENST00000513682.5:c.-31-2424del	ENSP00000427626.1:n.-31-2424del
ENST00000513952.5:c.-31-2424del	ENSP00000427218.1:n.-31-2424del
ENST00000514453.5:c.-31-2424del	ENSP00000425181.1:n.-31-2424del
ENST00000514546.5:c.-159-714del	ENSP00000425763.1:n.-159-714del
ENST00000515492.5:c.-51-5139del	ENSP00000425867.1:n.-51-5139del
ENST00000515740.5:c.-192-5136del	ENSP00000427039.1:n.-192-5136del
ENST00000515876.5:n.81-2424del
ENST00000622959.3:c.-620-2424del	ENSP00000485461.1:n.-620-2424del
NM_001297423.1:c.-738-2424del	NP_001284352.1:n.-738-2424del
NM_001297424.1:c.-54-5136del	NP_001284353.1:n.-54-5136del
NM_001297425.1:c.-51-5139del	NP_001284354.1:n.-51-5139del
NM_001297426.1:c.-620-2424del	NP_001284355.1:n.-620-2424del
NM_001297427.1:c.-876-2424del	NP_001284356.1:n.-876-2424del
NM_001297428.1:c.-192-5136del	NP_001284357.1:n.-192-5136del
NM_032326.3:c.-31-2424del	NP_115702.1:n.-31-2424del
XM_005272301.2:c.-31-2424del	XP_005272358.1:n.-31-2424del
XM_005272303.3:c.-482-2424del	XP_005272360.1:n.-482-2424del
XM_005272304.1:c.-415-2424del	XP_005272361.1:n.-415-2424del
XM_005272307.3:c.-31-2424del	XP_005272364.1:n.-31-2424del
XM_005272303.4:c.-482-2424del	XP_005272360.1:n.-482-2424del
XM_005272307.5:c.-31-2424del	XP_005272364.1:n.-31-2424del
XM_017008701.1:c.-159-714del	XP_016864190.1:n.-159-714del
XM_017008703.1:c.-866-714del	XP_016864192.1:n.-866-714del
XM_017008704.2:c.-738-2424del	XP_016864193.1:n.-738-2424del
XM_024454252.1:c.-839-2424del	XP_024310020.1:n.-839-2424del
XM_024454253.1:c.-1089-714del	XP_024310021.1:n.-1089-714del
XM_024454254.1:c.-1227-714del	XP_024310022.1:n.-1227-714del
XM_024454255.1:c.-192-5136del	XP_024310023.1:n.-192-5136del
NM_032326.4:c.-31-2424del MANE Select	NP_115702.1:n.-31-2424del
NM_001297423.2:c.-738-2424del	NP_001284352.1:n.-738-2424del
NM_001297424.2:c.-54-5136del	NP_001284353.1:n.-54-5136del
NM_001297425.2:c.-51-5139del	NP_001284354.1:n.-51-5139del
NM_001297427.2:c.-876-2424del	NP_001284356.1:n.-876-2424del
NM_001297428.2:c.-192-5136del	NP_001284357.1:n.-192-5136del
NM_001297426.2:c.-620-2424del	NP_001284355.1:n.-620-2424del