Canonical Allele Identifier: CA346073503
Gene: ASXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25742061T>C , CM000664.2:g.25742061T>C GRCh38
NC_000002.11:g.25964930T>C , CM000664.1:g.25964930T>C GRCh37
NC_000002.10:g.25818434T>C NCBI36
NG_052995.1:g.141456A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336112.9:c.4273A>G ENSP00000337250.5:p.Lys1425Glu
ENST00000435504.9:c.4276A>G MANE Select ENSP00000391447.3:p.Lys1426Glu
ENST00000336112.8:c.4192A>G ENSP00000337250.4:p.Lys1398Glu
ENST00000404843.5:c.2725A>G ENSP00000383920.1:p.Lys909Glu
ENST00000435504.8:c.4276A>G ENSP00000391447.3:p.Lys1426Glu
NM_018263.4:c.4276A>G NP_060733.4:p.Lys1426Glu
XM_006712039.2:c.3910A>G XP_006712102.1:p.Lys1304Glu
XM_006712040.1:c.3496A>G XP_006712103.1:p.Lys1166Glu
XM_011532950.1:c.4273A>G XP_011531252.1:p.Lys1425Glu
XM_011532951.1:c.4102A>G XP_011531253.1:p.Lys1368Glu
NM_018263.5:c.4276A>G NP_060733.4:p.Lys1426Glu
XM_006712039.3:c.3910A>G XP_006712102.1:p.Lys1304Glu
XM_006712040.2:c.3496A>G XP_006712103.1:p.Lys1166Glu
XM_011532950.3:c.4273A>G XP_011531252.1:p.Lys1425Glu
XM_011532951.2:c.4102A>G XP_011531253.1:p.Lys1368Glu
XM_017004430.1:c.3496A>G XP_016859919.1:p.Lys1166Glu
XM_024452974.1:c.4456A>G XP_024308742.1:p.Lys1486Glu
NM_001369346.1:c.4102A>G NP_001356275.1:p.Lys1368Glu
NM_001369347.1:c.3496A>G NP_001356276.1:p.Lys1166Glu
NM_018263.6:c.4276A>G MANE Select NP_060733.4:p.Lys1426Glu