Canonical Allele Identifier: CA402190777

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31324185G>T (hg19) ; chr18:g.33744221G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33744221G>T , CM000680.2:g.33744221G>T	GRCh38
NC_000018.9:g.31324185G>T , CM000680.1:g.31324185G>T	GRCh37
NC_000018.8:g.29578183G>T	NCBI36
NG_055244.1:g.170645G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696964.1:c.4376G>T	ENSP00000513003.1:p.Gly1459Val
ENST00000269197.12:c.4373G>T MANE Select	ENSP00000269197.4:p.Gly1458Val
ENST00000681521.1:c.4253G>T	ENSP00000506037.1:p.Gly1418Val
ENST00000269197.9:c.4373G>T	ENSP00000269197.4:p.Gly1458Val
NM_030632.1:c.4373G>T	NP_085135.1:p.Gly1458Val
XM_005258356.1:c.4376G>T	XP_005258413.1:p.Gly1459Val
XM_011526205.1:c.4349G>T	XP_011524507.1:p.Gly1450Val
XM_011526206.1:c.4295G>T	XP_011524508.1:p.Gly1432Val
XM_011526207.1:c.4295G>T	XP_011524509.1:p.Gly1432Val
XM_011526208.1:c.4256G>T	XP_011524510.1:p.Gly1419Val
XM_011526209.1:c.4205G>T	XP_011524511.1:p.Gly1402Val
XM_011526210.1:c.4205G>T	XP_011524512.1:p.Gly1402Val
XM_011526211.1:c.4205G>T	XP_011524513.1:p.Gly1402Val
XM_011526212.1:c.4205G>T	XP_011524514.1:p.Gly1402Val
XM_011526213.1:c.4205G>T	XP_011524515.1:p.Gly1402Val
XM_011526214.1:c.4205G>T	XP_011524516.1:p.Gly1402Val
XM_011526215.1:c.1337G>T	XP_011524517.1:p.Gly446Val
NM_030632.2:c.4373G>T	NP_085135.1:p.Gly1458Val
XM_011526205.2:c.4349G>T	XP_011524507.1:p.Gly1450Val
XM_011526206.2:c.4295G>T	XP_011524508.1:p.Gly1432Val
XM_011526213.2:c.4205G>T	XP_011524515.1:p.Gly1402Val
XM_017026012.1:c.4295G>T	XP_016881501.1:p.Gly1432Val
XM_017026013.1:c.4205G>T	XP_016881502.1:p.Gly1402Val
XM_017026014.2:c.4205G>T	XP_016881503.1:p.Gly1402Val
XM_024451269.1:c.4205G>T	XP_024307037.1:p.Gly1402Val
NM_030632.3:c.4373G>T MANE Select	NP_085135.1:p.Gly1458Val