Canonical Allele Identifier: CA2231553922

Gene: HP TXNL4B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72057415A= , CM000678.2:g.72057415A=	GRCh38
NC_000016.9:g.72091314A= , CM000678.1:g.72091314A=	GRCh37
NC_000016.8:g.70648815A=	NCBI36
NG_012651.1:g.7807A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005143.5:c.214A= (HP) MANE Select	NP_005134.1:p.Lys72=
ENST00000355906.10:c.214A= (HP) MANE Select	ENSP00000348170.5:p.Lys72=
NM_001126102.1:c.190+784A= (HP)	NP_001119574.1:n.190+784A=
NM_001126102.2:c.190+784A= (HP)	NP_001119574.1:n.190+784A=
NM_001126102.3:c.190+784A= (HP)	NP_001119574.1:n.190+784A=
NM_001318138.1:c.214A= (HP)	NP_001305067.1:p.Lys72=
NM_001318138.2:c.214A= (HP)	NP_001305067.1:p.Lys72=
NM_005143.3:c.214A= (HP)	NP_005134.1:p.Lys72=
NM_005143.4:c.214A= (HP)	NP_005134.1:p.Lys72=
ENST00000228226.12:c.19-839A= (HP)	ENSP00000228226.9:n.19-839A=
ENST00000355906.9:c.214A= (HP)	ENSP00000348170.5:p.Lys72=
ENST00000357763.8:c.214A= (HP)	ENSP00000350406.5:p.Lys72=
ENST00000398131.6:c.190+784A= (HP)	ENSP00000381199.2:n.190+784A=
ENST00000561927.3:n.209A= (HP)
ENST00000562153.5:c.285-13058T= (TXNL4B)	ENSP00000454635.1:n.285-13058T=
ENST00000562488.5:n.244A= (HP)
ENST00000562526.5:c.89-839A= (HP)	ENSP00000454413.1:n.89-839A=
ENST00000564499.5:c.89-839A= (HP)	ENSP00000456503.1:n.89-839A=
ENST00000565574.5:c.214A= (HP)	ENSP00000454966.1:p.Lys72=
ENST00000566821.1:n.2006+784A= (HP)
ENST00000567185.7:c.209A= (HP)
ENST00000567612.2:c.209A= (HP)
ENST00000568417.6:c.89-839A= (HP)	ENSP00000462662.1:n.89-839A=
ENST00000569639.5:c.89-839A= (HP)	ENSP00000463755.1:n.89-839A=
ENST00000570083.5:c.89-839A= (HP)	ENSP00000457629.1:n.89-839A=
ENST00000576168.6:c.209A= (HP)
ENST00000613898.1:c.94+810A= (HP)	ENSP00000478279.1:n.94+810A=
XM_005255922.3:c.214A= (HP)	XP_005255979.2:p.Lys72=
XM_017023377.2:c.285-13058T= (TXNL4B)	XP_016878866.1:n.285-13058T=