Canonical Allele Identifier: CA1363902877

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342740C= , CM000665.2:g.50342740C=	GRCh38
NC_000003.11:g.50380171C= , CM000665.1:g.50380171C=	GRCh37
NC_000003.10:g.50355175C=	NCBI36
NG_023270.1:g.3197G=
NG_042828.1:g.8007G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.701-171G= MANE Select	ENSP00000231749.3:n.701-171G=
ENST00000231749.7:c.701-171G=	ENSP00000231749.3:n.701-171G=
ENST00000360165.7:c.600-85G=	ENSP00000353289.3:n.600-85G=
ENST00000442887.1:c.572-171G=	ENSP00000393687.1:n.572-171G=
ENST00000443080.5:c.*453-171G=	ENSP00000415661.1:n.*453-171G=
ENST00000475688.1:n.429G=
NM_001308379.1:c.600-85G=	NP_001295308.1:n.600-85G=
NM_015896.2:c.701-171G=	NP_056980.2:n.701-171G=
NM_015896.3:c.701-171G=	NP_056980.2:n.701-171G=
XM_005265216.2:c.464-171G=	XP_005265273.1:n.464-171G=
XM_005265216.3:c.464-171G=	XP_005265273.1:n.464-171G=
NM_015896.4:c.701-171G= MANE Select	NP_056980.2:n.701-171G=
NM_001308379.2:c.600-85G=	NP_001295308.1:n.600-85G=