Canonical Allele Identifier: CA396676098

Gene: HP TXNL4B

Linked Data

• MyVariant Identifiers: chr16:g.72094022C>A (hg19) ; chr16:g.72060123C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72060123C>A , CM000678.2:g.72060123C>A	GRCh38
NC_000016.9:g.72094022C>A , CM000678.1:g.72094022C>A	GRCh37
NC_000016.8:g.70651523C>A	NCBI36
NG_012651.1:g.10515C>A
NG_030311.1:g.1898C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355906.10:c.454C>A (HP) MANE Select	ENSP00000348170.5:p.Pro152Thr
ENST00000228226.12:c.94-15C>A (HP)	ENSP00000228226.9:n.94-15C>A
ENST00000355906.9:c.454C>A (HP)	ENSP00000348170.5:p.Pro152Thr
ENST00000357763.8:c.562C>A (HP)	ENSP00000350406.5:p.Pro188Thr
ENST00000398131.6:c.277C>A (HP)	ENSP00000381199.2:p.Pro93Thr
ENST00000562153.5:c.285-15766G>T (TXNL4B)	ENSP00000454635.1:n.285-15766G>T
ENST00000562526.5:c.266-540C>A (HP)	ENSP00000454413.1:n.266-540C>A
ENST00000564499.5:c.266-109C>A (HP)	ENSP00000456503.1:n.266-109C>A
ENST00000565574.5:c.277C>A (HP)	ENSP00000454966.1:p.Pro93Thr
ENST00000566821.1:n.2093C>A (HP)
ENST00000567185.7:c.446C>A (HP)
ENST00000567612.2:c.438-109C>A (HP)
ENST00000570083.5:c.277C>A (HP)	ENSP00000457629.1:p.Pro93Thr
ENST00000613898.1:c.95-16C>A (HP)	ENSP00000478279.1:n.95-16C>A
NM_001126102.1:c.277C>A (HP)	NP_001119574.1:p.Pro93Thr
NM_005143.3:c.454C>A (HP)	NP_005134.1:p.Pro152Thr
XM_005255922.3:c.277C>A (HP)	XP_005255979.2:p.Pro93Thr
NM_001126102.2:c.277C>A (HP)	NP_001119574.1:p.Pro93Thr
NM_001318138.1:c.277C>A (HP)	NP_001305067.1:p.Pro93Thr
NM_005143.4:c.454C>A (HP)	NP_005134.1:p.Pro152Thr
XM_017023377.2:c.285-15766G>T (TXNL4B)	XP_016878866.1:n.285-15766G>T
NM_001318138.2:c.277C>A (HP)	NP_001305067.1:p.Pro93Thr
NM_005143.5:c.454C>A (HP) MANE Select	NP_005134.1:p.Pro152Thr
NM_001126102.3:c.277C>A (HP)	NP_001119574.1:p.Pro93Thr