Canonical Allele Identifier: CA503770656

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31324369G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33744405G>C , CM000680.2:g.33744405G>C	GRCh38
NC_000018.9:g.31324369G>C , CM000680.1:g.31324369G>C	GRCh37
NC_000018.8:g.29578367G>C	NCBI36
NG_055244.1:g.170829G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.4560G>C	ENSP00000513003.1:p.Val1520=
ENST00000269197.12:c.4557G>C MANE Select	ENSP00000269197.4:p.Val1519=
ENST00000681521.1:c.4437G>C	ENSP00000506037.1:p.Val1479=
ENST00000269197.9:c.4557G>C	ENSP00000269197.4:p.Val1519=
NM_030632.1:c.4557G>C	NP_085135.1:p.Val1519=
XM_005258356.1:c.4560G>C	XP_005258413.1:p.Val1520=
XM_011526205.1:c.4533G>C	XP_011524507.1:p.Val1511=
XM_011526206.1:c.4479G>C	XP_011524508.1:p.Val1493=
XM_011526207.1:c.4479G>C	XP_011524509.1:p.Val1493=
XM_011526208.1:c.4440G>C	XP_011524510.1:p.Val1480=
XM_011526209.1:c.4389G>C	XP_011524511.1:p.Val1463=
XM_011526210.1:c.4389G>C	XP_011524512.1:p.Val1463=
XM_011526211.1:c.4389G>C	XP_011524513.1:p.Val1463=
XM_011526212.1:c.4389G>C	XP_011524514.1:p.Val1463=
XM_011526213.1:c.4389G>C	XP_011524515.1:p.Val1463=
XM_011526214.1:c.4389G>C	XP_011524516.1:p.Val1463=
XM_011526215.1:c.1521G>C	XP_011524517.1:p.Val507=
NM_030632.2:c.4557G>C	NP_085135.1:p.Val1519=
XM_011526205.2:c.4533G>C	XP_011524507.1:p.Val1511=
XM_011526206.2:c.4479G>C	XP_011524508.1:p.Val1493=
XM_011526213.2:c.4389G>C	XP_011524515.1:p.Val1463=
XM_017026012.1:c.4479G>C	XP_016881501.1:p.Val1493=
XM_017026013.1:c.4389G>C	XP_016881502.1:p.Val1463=
XM_017026014.2:c.4389G>C	XP_016881503.1:p.Val1463=
XM_024451269.1:c.4389G>C	XP_024307037.1:p.Val1463=
NM_030632.3:c.4557G>C MANE Select	NP_085135.1:p.Val1519=