Canonical Allele Identifier: CA363655819

Gene: DAXX

Linked Data

• MyVariant Identifiers: chr6:g.33287987C>A (hg19) ; chr6:g.33320210C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33320210C>A , CM000668.2:g.33320210C>A	GRCh38
NC_000006.11:g.33287987C>A , CM000668.1:g.33287987C>A	GRCh37
NC_000006.10:g.33395965C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000706094.1:c.1302G>T	ENSP00000516212.1:p.Met434Ile
ENST00000374542.10:c.1266G>T MANE Select	ENSP00000363668.5:p.Met422Ile
ENST00000266000.10:c.1266G>T	ENSP00000266000.6:p.Met422Ile
ENST00000374542.9:c.1266G>T	ENSP00000363668.5:p.Met422Ile
ENST00000414083.6:c.1041G>T	ENSP00000396876.2:p.Met347Ile
ENST00000468536.5:n.296G>T
ENST00000477162.1:n.378G>T
ENST00000490173.1:n.251G>T
ENST00000620164.4:c.1266G>T	ENSP00000482399.1:p.Met422Ile
NM_001141969.1:c.1266G>T	NP_001135441.1:p.Met422Ile
NM_001141970.1:c.1302G>T	NP_001135442.1:p.Met434Ile
NM_001254717.1:c.1041G>T	NP_001241646.1:p.Met347Ile
NM_001350.4:c.1266G>T	NP_001341.1:p.Met422Ile
XM_005248860.3:c.162G>T	XP_005248917.1:p.Met54Ile
NM_001141969.2:c.1266G>T MANE Select	NP_001135441.1:p.Met422Ile
NM_001141970.2:c.1302G>T	NP_001135442.1:p.Met434Ile
NM_001350.5:c.1266G>T	NP_001341.1:p.Met422Ile
NM_001254717.2:c.1041G>T	NP_001241646.1:p.Met347Ile