Canonical Allele Identifier: CA1777402251

Gene: ASH2L

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38120214T>A , CM000670.2:g.38120214T>A	GRCh38
NC_000008.10:g.37977732T>A , CM000670.1:g.37977732T>A	GRCh37
NC_000008.9:g.38096889T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343823.11:c.948-718T>A MANE Select	ENSP00000340896.5:n.948-718T>A
ENST00000343823.10:c.948-718T>A	ENSP00000340896.5:n.948-718T>A
ENST00000428278.6:c.666-718T>A	ENSP00000395310.2:n.666-718T>A
ENST00000517496.5:c.*436-718T>A	ENSP00000430889.1:n.*436-718T>A
ENST00000518186.1:n.270-718T>A
ENST00000521652.5:c.666-718T>A	ENSP00000430259.1:n.666-718T>A
ENST00000545394.2:c.531-718T>A	ENSP00000443606.1:n.531-718T>A
NM_001105214.2:c.666-718T>A	NP_001098684.1:n.666-718T>A
NM_001261832.1:c.666-718T>A	NP_001248761.1:n.666-718T>A
NM_001282272.1:c.531-718T>A	NP_001269201.1:n.531-718T>A
NM_004674.4:c.948-718T>A	NP_004665.2:n.948-718T>A
XM_005273682.1:c.966-718T>A	XP_005273739.1:n.966-718T>A
XM_005273683.1:c.684-718T>A	XP_005273740.1:n.684-718T>A
XM_006716412.1:c.966-718T>A	XP_006716475.1:n.966-718T>A
XM_006716413.1:c.948-718T>A	XP_006716476.1:n.948-718T>A
XM_006716413.3:c.948-718T>A	XP_006716476.1:n.948-718T>A
NM_004674.5:c.948-718T>A MANE Select	NP_004665.2:n.948-718T>A