Canonical Allele Identifier: CA2634177600

Gene: HP TXNL4B

Linked Data

• gnomAD v4: 16-72060110-A-AGTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72060113_72060116dup , CM000678.2:g.72060113_72060116dup	GRCh38
NC_000016.9:g.72094012_72094015dup , CM000678.1:g.72094012_72094015dup	GRCh37
NC_000016.8:g.70651513_70651516dup	NCBI36
NG_012651.1:g.10505_10508dup
NG_030311.1:g.1888_1891dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355906.10:c.444_447dup (HP)
ENST00000228226.12:c.94-25_94-22dup (HP)	ENSP00000228226.9:n.94-25_94-22dup
ENST00000355906.9:c.444_447dup (HP)
ENST00000357763.8:c.552_555dup (HP)
ENST00000398131.6:c.267_270dup (HP)
ENST00000562153.5:c.285-15757_285-15754dup (TXNL4B)	ENSP00000454635.1:n.285-15757_285-15754dup
ENST00000562526.5:c.266-550_266-547dup (HP)	ENSP00000454413.1:n.266-550_266-547dup
ENST00000564499.5:c.266-119_266-116dup (HP)	ENSP00000456503.1:n.266-119_266-116dup
ENST00000565574.5:c.267_270dup (HP)
ENST00000566821.1:n.2083_2086dup (HP)
ENST00000567185.7:c.436_439dup (HP)
ENST00000567612.2:c.438-119_438-116dup (HP)
ENST00000570083.5:c.267_270dup (HP)
ENST00000613898.1:c.95-26_95-23dup (HP)	ENSP00000478279.1:n.95-26_95-23dup
NM_001126102.1:c.267_270dup (HP)
NM_005143.3:c.444_447dup (HP)
XM_005255922.3:c.267_270dup (HP)
NM_001126102.2:c.267_270dup (HP)
NM_001318138.1:c.267_270dup (HP)
NM_005143.4:c.444_447dup (HP)
XM_017023377.2:c.285-15757_285-15754dup (TXNL4B)	XP_016878866.1:n.285-15757_285-15754dup
NM_001318138.2:c.267_270dup (HP)
NM_005143.5:c.444_447dup (HP)
NM_001126102.3:c.267_270dup (HP)