Canonical Allele Identifier: CA402190533
Gene: ASXL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33744107T>A , CM000680.2:g.33744107T>A GRCh38
NC_000018.9:g.31324071T>A , CM000680.1:g.31324071T>A GRCh37
NC_000018.8:g.29578069T>A NCBI36
NG_055244.1:g.170531T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696964.1:c.4262T>A ENSP00000513003.1:p.Met1421Lys
ENST00000269197.12:c.4259T>A MANE Select ENSP00000269197.4:p.Met1420Lys
ENST00000681521.1:c.4139T>A ENSP00000506037.1:p.Met1380Lys
ENST00000269197.9:c.4259T>A ENSP00000269197.4:p.Met1420Lys
NM_030632.1:c.4259T>A NP_085135.1:p.Met1420Lys
XM_005258356.1:c.4262T>A XP_005258413.1:p.Met1421Lys
XM_011526205.1:c.4235T>A XP_011524507.1:p.Met1412Lys
XM_011526206.1:c.4181T>A XP_011524508.1:p.Met1394Lys
XM_011526207.1:c.4181T>A XP_011524509.1:p.Met1394Lys
XM_011526208.1:c.4142T>A XP_011524510.1:p.Met1381Lys
XM_011526209.1:c.4091T>A XP_011524511.1:p.Met1364Lys
XM_011526210.1:c.4091T>A XP_011524512.1:p.Met1364Lys
XM_011526211.1:c.4091T>A XP_011524513.1:p.Met1364Lys
XM_011526212.1:c.4091T>A XP_011524514.1:p.Met1364Lys
XM_011526213.1:c.4091T>A XP_011524515.1:p.Met1364Lys
XM_011526214.1:c.4091T>A XP_011524516.1:p.Met1364Lys
XM_011526215.1:c.1223T>A XP_011524517.1:p.Met408Lys
NM_030632.2:c.4259T>A NP_085135.1:p.Met1420Lys
XM_011526205.2:c.4235T>A XP_011524507.1:p.Met1412Lys
XM_011526206.2:c.4181T>A XP_011524508.1:p.Met1394Lys
XM_011526213.2:c.4091T>A XP_011524515.1:p.Met1364Lys
XM_017026012.1:c.4181T>A XP_016881501.1:p.Met1394Lys
XM_017026013.1:c.4091T>A XP_016881502.1:p.Met1364Lys
XM_017026014.2:c.4091T>A XP_016881503.1:p.Met1364Lys
XM_024451269.1:c.4091T>A XP_024307037.1:p.Met1364Lys
NM_030632.3:c.4259T>A MANE Select NP_085135.1:p.Met1420Lys