Canonical Allele Identifier: CA2231555295

Gene: HP TXNL4B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72060498C= , CM000678.2:g.72060498C=	GRCh38
NC_000016.9:g.72094397C= , CM000678.1:g.72094397C=	GRCh37
NC_000016.8:g.70651898C=	NCBI36
NG_012651.1:g.10890C=
NG_030311.1:g.2273C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355906.10:c.829C= (HP) MANE Select	ENSP00000348170.5:p.Arg277=
ENST00000228226.12:c.454C= (HP)	ENSP00000228226.9:p.Arg152=
ENST00000355906.9:c.829C= (HP)	ENSP00000348170.5:p.Arg277=
ENST00000357763.8:c.937C= (HP)	ENSP00000350406.5:p.Arg313=
ENST00000398131.6:c.652C= (HP)	ENSP00000381199.2:p.Arg218=
ENST00000562153.5:c.285-16141G= (TXNL4B)	ENSP00000454635.1:n.285-16141G=
ENST00000562526.5:c.266-165C= (HP)	ENSP00000454413.1:n.266-165C=
ENST00000564499.5:c.532C= (HP)	ENSP00000456503.1:p.Arg178=
ENST00000565574.5:c.652C= (HP)	ENSP00000454966.1:p.Arg218=
ENST00000566821.1:n.2468C= (HP)
ENST00000567185.7:c.821C= (HP)
ENST00000567612.2:c.704C= (HP)
ENST00000570083.5:c.652C= (HP)	ENSP00000457629.1:p.Arg218=
ENST00000613898.1:c.454C= (HP)	ENSP00000478279.1:p.Arg152=
NM_001126102.1:c.652C= (HP)	NP_001119574.1:p.Arg218=
NM_005143.3:c.829C= (HP)	NP_005134.1:p.Arg277=
XM_005255922.3:c.652C= (HP)	XP_005255979.2:p.Arg218=
NM_001126102.2:c.652C= (HP)	NP_001119574.1:p.Arg218=
NM_001318138.1:c.652C= (HP)	NP_001305067.1:p.Arg218=
NM_005143.4:c.829C= (HP)	NP_005134.1:p.Arg277=
XM_017023377.2:c.285-16141G= (TXNL4B)	XP_016878866.1:n.285-16141G=
NM_001318138.2:c.652C= (HP)	NP_001305067.1:p.Arg218=
NM_005143.5:c.829C= (HP) MANE Select	NP_005134.1:p.Arg277=
NM_001126102.3:c.652C= (HP)	NP_001119574.1:p.Arg218=