Canonical Allele Identifier: CA1363902854

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342709_50342710delinsAC , CM000665.2:g.50342709_50342710delinsAC	GRCh38
NC_000003.11:g.50380140_50380141delinsAC , CM000665.1:g.50380140_50380141delinsAC	GRCh37
NC_000003.10:g.50355144_50355145delinsAC	NCBI36
NG_023270.1:g.3227_3228delinsGT
NG_042828.1:g.8037_8038delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.701-141_701-140delinsGT MANE Select	ENSP00000231749.3:n.701-141_701-140delinsGT
ENST00000231749.7:c.701-141_701-140delinsGT	ENSP00000231749.3:n.701-141_701-140delinsGT
ENST00000360165.7:c.600-55_600-54delinsGT	ENSP00000353289.3:n.600-55_600-54delinsGT
ENST00000442887.1:c.572-141_572-140delinsGT	ENSP00000393687.1:n.572-141_572-140delinsGT
ENST00000443080.5:c.*453-141_*453-140delinsGT	ENSP00000415661.1:n.*453-141_*453-140delinsGT
ENST00000475688.1:n.459_460delinsGT
NM_001308379.1:c.600-55_600-54delinsGT	NP_001295308.1:n.600-55_600-54delinsGT
NM_015896.2:c.701-141_701-140delinsGT	NP_056980.2:n.701-141_701-140delinsGT
NM_015896.3:c.701-141_701-140delinsGT	NP_056980.2:n.701-141_701-140delinsGT
XM_005265216.2:c.464-141_464-140delinsGT	XP_005265273.1:n.464-141_464-140delinsGT
XM_005265216.3:c.464-141_464-140delinsGT	XP_005265273.1:n.464-141_464-140delinsGT
NM_015896.4:c.701-141_701-140delinsGT MANE Select	NP_056980.2:n.701-141_701-140delinsGT
NM_001308379.2:c.600-55_600-54delinsGT	NP_001295308.1:n.600-55_600-54delinsGT