Canonical Allele Identifier: CA1777417171

Gene: ASH2L

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38138724A= , CM000670.2:g.38138724A=	GRCh38
NC_000008.10:g.37996242A= , CM000670.1:g.37996242A=	GRCh37
NC_000008.9:g.38115399A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343823.11:c.1720-92A= MANE Select	ENSP00000340896.5:n.1720-92A=
ENST00000343823.10:c.1720-92A=	ENSP00000340896.5:n.1720-92A=
ENST00000428278.6:c.1438-92A=	ENSP00000395310.2:n.1438-92A=
ENST00000517496.5:c.*1208-92A=	ENSP00000430889.1:n.*1208-92A=
ENST00000520079.1:n.1230A=
ENST00000521652.5:c.1339-92A=	ENSP00000430259.1:n.1339-92A=
ENST00000521808.5:c.104-92A=
ENST00000524247.5:c.506-92A=
ENST00000545394.2:c.1303-92A=	ENSP00000443606.1:n.1303-92A=
NM_001105214.2:c.1438-92A=	NP_001098684.1:n.1438-92A=
NM_001261832.1:c.1339-92A=	NP_001248761.1:n.1339-92A=
NM_001282272.1:c.1303-92A=	NP_001269201.1:n.1303-92A=
NM_004674.4:c.1720-92A=	NP_004665.2:n.1720-92A=
XM_005273682.1:c.1738-92A=	XP_005273739.1:n.1738-92A=
XM_005273683.1:c.1456-92A=	XP_005273740.1:n.1456-92A=
XM_006716412.1:c.1639-92A=	XP_006716475.1:n.1639-92A=
XM_006716413.1:c.1621-92A=	XP_006716476.1:n.1621-92A=
XM_006716413.3:c.1621-92A=	XP_006716476.1:n.1621-92A=
NM_004674.5:c.1720-92A= MANE Select	NP_004665.2:n.1720-92A=