Canonical Allele Identifier: CA496415060

Gene: HP TXNL4B

Linked Data

• MyVariant Identifiers: chr16:g.72094477G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72060578G>T , CM000678.2:g.72060578G>T	GRCh38
NC_000016.9:g.72094477G>T , CM000678.1:g.72094477G>T	GRCh37
NC_000016.8:g.70651978G>T	NCBI36
NG_012651.1:g.10970G>T
NG_030311.1:g.2353G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355906.10:c.909G>T (HP) MANE Select	ENSP00000348170.5:p.Val303=
ENST00000228226.12:c.534G>T (HP)	ENSP00000228226.9:p.Val178=
ENST00000355906.9:c.909G>T (HP)	ENSP00000348170.5:p.Val303=
ENST00000357763.8:c.1017G>T (HP)	ENSP00000350406.5:p.Val339=
ENST00000398131.6:c.732G>T (HP)	ENSP00000381199.2:p.Val244=
ENST00000562153.5:c.285-16221C>A (TXNL4B)	ENSP00000454635.1:n.285-16221C>A
ENST00000562526.5:c.266-85G>T (HP)	ENSP00000454413.1:n.266-85G>T
ENST00000564499.5:c.612G>T (HP)	ENSP00000456503.1:p.Val204=
ENST00000565574.5:c.732G>T (HP)	ENSP00000454966.1:p.Val244=
ENST00000566821.1:n.2548G>T (HP)
ENST00000567185.7:c.901G>T (HP)
ENST00000567612.2:c.784G>T (HP)
ENST00000570083.5:c.732G>T (HP)	ENSP00000457629.1:p.Val244=
ENST00000613898.1:c.534G>T (HP)	ENSP00000478279.1:p.Val178=
NM_001126102.1:c.732G>T (HP)	NP_001119574.1:p.Val244=
NM_005143.3:c.909G>T (HP)	NP_005134.1:p.Val303=
XM_005255922.3:c.732G>T (HP)	XP_005255979.2:p.Val244=
NM_001126102.2:c.732G>T (HP)	NP_001119574.1:p.Val244=
NM_001318138.1:c.732G>T (HP)	NP_001305067.1:p.Val244=
NM_005143.4:c.909G>T (HP)	NP_005134.1:p.Val303=
XM_017023377.2:c.285-16221C>A (TXNL4B)	XP_016878866.1:n.285-16221C>A
NM_001318138.2:c.732G>T (HP)	NP_001305067.1:p.Val244=
NM_005143.5:c.909G>T (HP) MANE Select	NP_005134.1:p.Val303=
NM_001126102.3:c.732G>T (HP)	NP_001119574.1:p.Val244=