Canonical Allele Identifier: CA2231555265

Gene: HP TXNL4B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72060438T= , CM000678.2:g.72060438T=	GRCh38
NC_000016.9:g.72094337T= , CM000678.1:g.72094337T=	GRCh37
NC_000016.8:g.70651838T=	NCBI36
NG_012651.1:g.10830T=
NG_030311.1:g.2213T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355906.10:c.769T= (HP) MANE Select	ENSP00000348170.5:p.Ser257=
ENST00000228226.12:c.394T= (HP)	ENSP00000228226.9:p.Ser132=
ENST00000355906.9:c.769T= (HP)	ENSP00000348170.5:p.Ser257=
ENST00000357763.8:c.877T= (HP)	ENSP00000350406.5:p.Ser293=
ENST00000398131.6:c.592T= (HP)	ENSP00000381199.2:p.Ser198=
ENST00000562153.5:c.285-16081A= (TXNL4B)	ENSP00000454635.1:n.285-16081A=
ENST00000562526.5:c.266-225T= (HP)	ENSP00000454413.1:n.266-225T=
ENST00000564499.5:c.472T= (HP)	ENSP00000456503.1:p.Ser158=
ENST00000565574.5:c.592T= (HP)	ENSP00000454966.1:p.Ser198=
ENST00000566821.1:n.2408T= (HP)
ENST00000567185.7:c.761T= (HP)
ENST00000567612.2:c.644T= (HP)
ENST00000570083.5:c.592T= (HP)	ENSP00000457629.1:p.Ser198=
ENST00000613898.1:c.394T= (HP)	ENSP00000478279.1:p.Ser132=
NM_001126102.1:c.592T= (HP)	NP_001119574.1:p.Ser198=
NM_005143.3:c.769T= (HP)	NP_005134.1:p.Ser257=
XM_005255922.3:c.592T= (HP)	XP_005255979.2:p.Ser198=
NM_001126102.2:c.592T= (HP)	NP_001119574.1:p.Ser198=
NM_001318138.1:c.592T= (HP)	NP_001305067.1:p.Ser198=
NM_005143.4:c.769T= (HP)	NP_005134.1:p.Ser257=
XM_017023377.2:c.285-16081A= (TXNL4B)	XP_016878866.1:n.285-16081A=
NM_001318138.2:c.592T= (HP)	NP_001305067.1:p.Ser198=
NM_005143.5:c.769T= (HP) MANE Select	NP_005134.1:p.Ser257=
NM_001126102.3:c.592T= (HP)	NP_001119574.1:p.Ser198=