Canonical Allele Identifier: CA363655765

Gene: DAXX

Linked Data

• MyVariant Identifiers: chr6:g.33287980G>A (hg19) ; chr6:g.33320203G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33320203G>A , CM000668.2:g.33320203G>A	GRCh38
NC_000006.11:g.33287980G>A , CM000668.1:g.33287980G>A	GRCh37
NC_000006.10:g.33395958G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000706094.1:c.1309C>T	ENSP00000516212.1:p.Gln437Ter
ENST00000374542.10:c.1273C>T MANE Select	ENSP00000363668.5:p.Gln425Ter
ENST00000266000.10:c.1273C>T	ENSP00000266000.6:p.Gln425Ter
ENST00000374542.9:c.1273C>T	ENSP00000363668.5:p.Gln425Ter
ENST00000414083.6:c.1048C>T	ENSP00000396876.2:p.Gln350Ter
ENST00000468536.5:n.303C>T
ENST00000477162.1:n.385C>T
ENST00000490173.1:n.258C>T
ENST00000620164.4:c.1273C>T	ENSP00000482399.1:p.Gln425Ter
NM_001141969.1:c.1273C>T	NP_001135441.1:p.Gln425Ter
NM_001141970.1:c.1309C>T	NP_001135442.1:p.Gln437Ter
NM_001254717.1:c.1048C>T	NP_001241646.1:p.Gln350Ter
NM_001350.4:c.1273C>T	NP_001341.1:p.Gln425Ter
XM_005248860.3:c.169C>T	XP_005248917.1:p.Gln57Ter
NM_001141969.2:c.1273C>T MANE Select	NP_001135441.1:p.Gln425Ter
NM_001141970.2:c.1309C>T	NP_001135442.1:p.Gln437Ter
NM_001350.5:c.1273C>T	NP_001341.1:p.Gln425Ter
NM_001254717.2:c.1048C>T	NP_001241646.1:p.Gln350Ter