Canonical Allele Identifier: CA503769481

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31322974C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743010C>G , CM000680.2:g.33743010C>G	GRCh38
NC_000018.9:g.31322974C>G , CM000680.1:g.31322974C>G	GRCh37
NC_000018.8:g.29576972C>G	NCBI36
NG_055244.1:g.169434C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.3165C>G	ENSP00000513003.1:p.Leu1055=
ENST00000269197.12:c.3162C>G MANE Select	ENSP00000269197.4:p.Leu1054=
ENST00000592288.6:c.*2286C>G	ENSP00000465053.1:n.*2286C>G
ENST00000592541.6:c.*2821C>G	ENSP00000466655.2:n.*2821C>G
ENST00000593195.6:c.3374C>G	ENSP00000466073.1:n.3374C>G
ENST00000642541.1:c.2994C>G	ENSP00000493665.1:p.Leu998=
ENST00000681521.1:c.3042C>G	ENSP00000506037.1:p.Leu1014=
ENST00000269197.9:c.3162C>G	ENSP00000269197.4:p.Leu1054=
ENST00000592288.5:c.*2286C>G	ENSP00000465053.1:n.*2286C>G
NM_030632.1:c.3162C>G	NP_085135.1:p.Leu1054=
XM_005258356.1:c.3165C>G	XP_005258413.1:p.Leu1055=
XM_011526205.1:c.3138C>G	XP_011524507.1:p.Leu1046=
XM_011526206.1:c.3084C>G	XP_011524508.1:p.Leu1028=
XM_011526207.1:c.3084C>G	XP_011524509.1:p.Leu1028=
XM_011526208.1:c.3045C>G	XP_011524510.1:p.Leu1015=
XM_011526209.1:c.2994C>G	XP_011524511.1:p.Leu998=
XM_011526210.1:c.2994C>G	XP_011524512.1:p.Leu998=
XM_011526211.1:c.2994C>G	XP_011524513.1:p.Leu998=
XM_011526212.1:c.2994C>G	XP_011524514.1:p.Leu998=
XM_011526213.1:c.2994C>G	XP_011524515.1:p.Leu998=
XM_011526214.1:c.2994C>G	XP_011524516.1:p.Leu998=
XM_011526215.1:c.126C>G	XP_011524517.1:p.Leu42=
NM_030632.2:c.3162C>G	NP_085135.1:p.Leu1054=
XM_011526205.2:c.3138C>G	XP_011524507.1:p.Leu1046=
XM_011526206.2:c.3084C>G	XP_011524508.1:p.Leu1028=
XM_011526213.2:c.2994C>G	XP_011524515.1:p.Leu998=
XM_017026012.1:c.3084C>G	XP_016881501.1:p.Leu1028=
XM_017026013.1:c.2994C>G	XP_016881502.1:p.Leu998=
XM_017026014.2:c.2994C>G	XP_016881503.1:p.Leu998=
XM_024451269.1:c.2994C>G	XP_024307037.1:p.Leu998=
NM_030632.3:c.3162C>G MANE Select	NP_085135.1:p.Leu1054=