Canonical Allele Identifier: CA1777417235

Gene: ASH2L

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38138822A= , CM000670.2:g.38138822A=	GRCh38
NC_000008.10:g.37996340A= , CM000670.1:g.37996340A=	GRCh37
NC_000008.9:g.38115497A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343823.11:c.1726A= MANE Select	ENSP00000340896.5:p.Ile576=
ENST00000343823.10:c.1726A=	ENSP00000340896.5:p.Ile576=
ENST00000428278.6:c.1444A=	ENSP00000395310.2:p.Ile482=
ENST00000517496.5:c.*1214A=	ENSP00000430889.1:n.*1214A=
ENST00000520079.1:n.1328A=
ENST00000521652.5:c.1345A=	ENSP00000430259.1:p.Ile449=
ENST00000521808.5:c.110A=
ENST00000524247.5:c.512A=
ENST00000545394.2:c.1309A=	ENSP00000443606.1:p.Ile437=
NM_001105214.2:c.1444A=	NP_001098684.1:p.Ile482=
NM_001261832.1:c.1345A=	NP_001248761.1:p.Ile449=
NM_001282272.1:c.1309A=	NP_001269201.1:p.Ile437=
NM_004674.4:c.1726A=	NP_004665.2:p.Ile576=
XM_005273682.1:c.1744A=	XP_005273739.1:p.Ile582=
XM_005273683.1:c.1462A=	XP_005273740.1:p.Ile488=
XM_006716412.1:c.1645A=	XP_006716475.1:p.Ile549=
XM_006716413.1:c.1627A=	XP_006716476.1:p.Ile543=
XM_006716413.3:c.1627A=	XP_006716476.1:p.Ile543=
NM_004674.5:c.1726A= MANE Select	NP_004665.2:p.Ile576=