Canonical Allele Identifier: CA496299126

Gene: HP TXNL4B

Linked Data

• gnomAD v4: 16-72060113-A-G
• MyVariant Identifiers: chr16:g.72094012A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72060113A>G , CM000678.2:g.72060113A>G	GRCh38
NC_000016.9:g.72094012A>G , CM000678.1:g.72094012A>G	GRCh37
NC_000016.8:g.70651513A>G	NCBI36
NG_012651.1:g.10505A>G
NG_030311.1:g.1888A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355906.10:c.444A>G (HP) MANE Select	ENSP00000348170.5:p.Val148=
ENST00000228226.12:c.94-25A>G (HP)	ENSP00000228226.9:n.94-25A>G
ENST00000355906.9:c.444A>G (HP)	ENSP00000348170.5:p.Val148=
ENST00000357763.8:c.552A>G (HP)	ENSP00000350406.5:p.Val184=
ENST00000398131.6:c.267A>G (HP)	ENSP00000381199.2:p.Val89=
ENST00000562153.5:c.285-15756T>C (TXNL4B)	ENSP00000454635.1:n.285-15756T>C
ENST00000562526.5:c.266-550A>G (HP)	ENSP00000454413.1:n.266-550A>G
ENST00000564499.5:c.266-119A>G (HP)	ENSP00000456503.1:n.266-119A>G
ENST00000565574.5:c.267A>G (HP)	ENSP00000454966.1:p.Val89=
ENST00000566821.1:n.2083A>G (HP)
ENST00000567185.7:c.436A>G (HP)
ENST00000567612.2:c.438-119A>G (HP)
ENST00000570083.5:c.267A>G (HP)	ENSP00000457629.1:p.Val89=
ENST00000613898.1:c.95-26A>G (HP)	ENSP00000478279.1:n.95-26A>G
NM_001126102.1:c.267A>G (HP)	NP_001119574.1:p.Val89=
NM_005143.3:c.444A>G (HP)	NP_005134.1:p.Val148=
XM_005255922.3:c.267A>G (HP)	XP_005255979.2:p.Val89=
NM_001126102.2:c.267A>G (HP)	NP_001119574.1:p.Val89=
NM_001318138.1:c.267A>G (HP)	NP_001305067.1:p.Val89=
NM_005143.4:c.444A>G (HP)	NP_005134.1:p.Val148=
XM_017023377.2:c.285-15756T>C (TXNL4B)	XP_016878866.1:n.285-15756T>C
NM_001318138.2:c.267A>G (HP)	NP_001305067.1:p.Val89=
NM_005143.5:c.444A>G (HP) MANE Select	NP_005134.1:p.Val148=
NM_001126102.3:c.267A>G (HP)	NP_001119574.1:p.Val89=