Canonical Allele Identifier: CA450110111

Gene: DAXX

Linked Data

• MyVariant Identifiers: chr6:g.33287984T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33320207T>A , CM000668.2:g.33320207T>A	GRCh38
NC_000006.11:g.33287984T>A , CM000668.1:g.33287984T>A	GRCh37
NC_000006.10:g.33395962T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000706094.1:c.1305A>T	ENSP00000516212.1:p.Ala435=
ENST00000374542.10:c.1269A>T MANE Select	ENSP00000363668.5:p.Ala423=
ENST00000266000.10:c.1269A>T	ENSP00000266000.6:p.Ala423=
ENST00000374542.9:c.1269A>T	ENSP00000363668.5:p.Ala423=
ENST00000414083.6:c.1044A>T	ENSP00000396876.2:p.Ala348=
ENST00000468536.5:n.299A>T
ENST00000477162.1:n.381A>T
ENST00000490173.1:n.254A>T
ENST00000620164.4:c.1269A>T	ENSP00000482399.1:p.Ala423=
NM_001141969.1:c.1269A>T	NP_001135441.1:p.Ala423=
NM_001141970.1:c.1305A>T	NP_001135442.1:p.Ala435=
NM_001254717.1:c.1044A>T	NP_001241646.1:p.Ala348=
NM_001350.4:c.1269A>T	NP_001341.1:p.Ala423=
XM_005248860.3:c.165A>T	XP_005248917.1:p.Ala55=
NM_001141969.2:c.1269A>T MANE Select	NP_001135441.1:p.Ala423=
NM_001141970.2:c.1305A>T	NP_001135442.1:p.Ala435=
NM_001350.5:c.1269A>T	NP_001341.1:p.Ala423=
NM_001254717.2:c.1044A>T	NP_001241646.1:p.Ala348=