Canonical Allele Identifier: CA2231555131

Gene: HP TXNL4B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72060160G= , CM000678.2:g.72060160G=	GRCh38
NC_000016.9:g.72094059G= , CM000678.1:g.72094059G=	GRCh37
NC_000016.8:g.70651560G=	NCBI36
NG_012651.1:g.10552G=
NG_030311.1:g.1935G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355906.10:c.491G= (HP) MANE Select	ENSP00000348170.5:p.Gly164=
ENST00000228226.12:c.116G= (HP)	ENSP00000228226.9:p.Gly39=
ENST00000355906.9:c.491G= (HP)	ENSP00000348170.5:p.Gly164=
ENST00000357763.8:c.599G= (HP)	ENSP00000350406.5:p.Gly200=
ENST00000398131.6:c.314G= (HP)	ENSP00000381199.2:p.Gly105=
ENST00000562153.5:c.285-15803C= (TXNL4B)	ENSP00000454635.1:n.285-15803C=
ENST00000562526.5:c.266-503G= (HP)	ENSP00000454413.1:n.266-503G=
ENST00000564499.5:c.266-72G= (HP)	ENSP00000456503.1:n.266-72G=
ENST00000565574.5:c.314G= (HP)	ENSP00000454966.1:p.Gly105=
ENST00000566821.1:n.2130G= (HP)
ENST00000567185.7:c.483G= (HP)
ENST00000567612.2:c.438-72G= (HP)
ENST00000570083.5:c.314G= (HP)	ENSP00000457629.1:p.Gly105=
ENST00000613898.1:c.116G= (HP)	ENSP00000478279.1:p.Gly39=
NM_001126102.1:c.314G= (HP)	NP_001119574.1:p.Gly105=
NM_005143.3:c.491G= (HP)	NP_005134.1:p.Gly164=
XM_005255922.3:c.314G= (HP)	XP_005255979.2:p.Gly105=
NM_001126102.2:c.314G= (HP)	NP_001119574.1:p.Gly105=
NM_001318138.1:c.314G= (HP)	NP_001305067.1:p.Gly105=
NM_005143.4:c.491G= (HP)	NP_005134.1:p.Gly164=
XM_017023377.2:c.285-15803C= (TXNL4B)	XP_016878866.1:n.285-15803C=
NM_001318138.2:c.314G= (HP)	NP_001305067.1:p.Gly105=
NM_005143.5:c.491G= (HP) MANE Select	NP_005134.1:p.Gly164=
NM_001126102.3:c.314G= (HP)	NP_001119574.1:p.Gly105=