Canonical Allele Identifier: CA2231555138

Gene: HP TXNL4B

Linked Data

• dbSNP Id: rs2041519071

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72060169_72060170insCTAT , CM000678.2:g.72060169_72060170insCTAT	GRCh38
NC_000016.9:g.72094068_72094069insCTAT , CM000678.1:g.72094068_72094069insCTAT	GRCh37
NC_000016.8:g.70651569_70651570insCTAT	NCBI36
NG_012651.1:g.10561_10562insCTAT
NG_030311.1:g.1944_1945insCTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355906.10:c.500_501insCTAT (HP) MANE Select	ENSP00000348170.5:p.Asp168TyrfsTer12
ENST00000228226.12:c.125_126insCTAT (HP)	ENSP00000228226.9:p.Asp43TyrfsTer12
ENST00000355906.9:c.500_501insCTAT (HP)	ENSP00000348170.5:p.Asp168TyrfsTer12
ENST00000357763.8:c.608_609insCTAT (HP)	ENSP00000350406.5:p.Asp204TyrfsTer12
ENST00000398131.6:c.323_324insCTAT (HP)	ENSP00000381199.2:p.Asp109TyrfsTer12
ENST00000562153.5:c.285-15812_285-15811insTAGA (TXNL4B)	ENSP00000454635.1:n.285-15812_285-15811insTAGA
ENST00000562526.5:c.266-494_266-493insCTAT (HP)	ENSP00000454413.1:n.266-494_266-493insCTAT
ENST00000564499.5:c.266-63_266-62insCTAT (HP)	ENSP00000456503.1:n.266-63_266-62insCTAT
ENST00000565574.5:c.323_324insCTAT (HP)	ENSP00000454966.1:p.Asp109TyrfsTer12
ENST00000566821.1:n.2139_2140insCTAT (HP)
ENST00000567185.7:c.492_493insCTAT (HP)
ENST00000567612.2:c.438-63_438-62insCTAT (HP)
ENST00000570083.5:c.323_324insCTAT (HP)	ENSP00000457629.1:p.Asp109TyrfsTer12
ENST00000613898.1:c.125_126insCTAT (HP)	ENSP00000478279.1:p.Asp43TyrfsTer12
NM_001126102.1:c.323_324insCTAT (HP)	NP_001119574.1:p.Asp109TyrfsTer12
NM_005143.3:c.500_501insCTAT (HP)	NP_005134.1:p.Asp168TyrfsTer12
XM_005255922.3:c.323_324insCTAT (HP)	XP_005255979.2:p.Asp109TyrfsTer12
NM_001126102.2:c.323_324insCTAT (HP)	NP_001119574.1:p.Asp109TyrfsTer12
NM_001318138.1:c.323_324insCTAT (HP)	NP_001305067.1:p.Asp109TyrfsTer12
NM_005143.4:c.500_501insCTAT (HP)	NP_005134.1:p.Asp168TyrfsTer12
XM_017023377.2:c.285-15812_285-15811insTAGA (TXNL4B)	XP_016878866.1:n.285-15812_285-15811insTAGA
NM_001318138.2:c.323_324insCTAT (HP)	NP_001305067.1:p.Asp109TyrfsTer12
NM_005143.5:c.500_501insCTAT (HP) MANE Select	NP_005134.1:p.Asp168TyrfsTer12
NM_001126102.3:c.323_324insCTAT (HP)	NP_001119574.1:p.Asp109TyrfsTer12