Canonical Allele Identifier: CA402191574

Gene: ASXL3

Linked Data

• gnomAD v4: 18-33744518-C-T
• MyVariant Identifiers: chr18:g.31324482C>T (hg19) ; chr18:g.33744518C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33744518C>T , CM000680.2:g.33744518C>T	GRCh38
NC_000018.9:g.31324482C>T , CM000680.1:g.31324482C>T	GRCh37
NC_000018.8:g.29578480C>T	NCBI36
NG_055244.1:g.170942C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.4673C>T	ENSP00000513003.1:p.Thr1558Ile
ENST00000269197.12:c.4670C>T MANE Select	ENSP00000269197.4:p.Thr1557Ile
ENST00000681521.1:c.4550C>T	ENSP00000506037.1:p.Thr1517Ile
ENST00000269197.9:c.4670C>T	ENSP00000269197.4:p.Thr1557Ile
NM_030632.1:c.4670C>T	NP_085135.1:p.Thr1557Ile
XM_005258356.1:c.4673C>T	XP_005258413.1:p.Thr1558Ile
XM_011526205.1:c.4646C>T	XP_011524507.1:p.Thr1549Ile
XM_011526206.1:c.4592C>T	XP_011524508.1:p.Thr1531Ile
XM_011526207.1:c.4592C>T	XP_011524509.1:p.Thr1531Ile
XM_011526208.1:c.4553C>T	XP_011524510.1:p.Thr1518Ile
XM_011526209.1:c.4502C>T	XP_011524511.1:p.Thr1501Ile
XM_011526210.1:c.4502C>T	XP_011524512.1:p.Thr1501Ile
XM_011526211.1:c.4502C>T	XP_011524513.1:p.Thr1501Ile
XM_011526212.1:c.4502C>T	XP_011524514.1:p.Thr1501Ile
XM_011526213.1:c.4502C>T	XP_011524515.1:p.Thr1501Ile
XM_011526214.1:c.4502C>T	XP_011524516.1:p.Thr1501Ile
XM_011526215.1:c.1634C>T	XP_011524517.1:p.Thr545Ile
NM_030632.2:c.4670C>T	NP_085135.1:p.Thr1557Ile
XM_011526205.2:c.4646C>T	XP_011524507.1:p.Thr1549Ile
XM_011526206.2:c.4592C>T	XP_011524508.1:p.Thr1531Ile
XM_011526213.2:c.4502C>T	XP_011524515.1:p.Thr1501Ile
XM_017026012.1:c.4592C>T	XP_016881501.1:p.Thr1531Ile
XM_017026013.1:c.4502C>T	XP_016881502.1:p.Thr1501Ile
XM_017026014.2:c.4502C>T	XP_016881503.1:p.Thr1501Ile
XM_024451269.1:c.4502C>T	XP_024307037.1:p.Thr1501Ile
NM_030632.3:c.4670C>T MANE Select	NP_085135.1:p.Thr1557Ile