Canonical Allele Identifier: CA2416926

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50341486C>A , CM000665.2:g.50341486C>A	GRCh38
NC_000003.11:g.50378917C>A , CM000665.1:g.50378917C>A	GRCh37
NC_000003.10:g.50353921C>A	NCBI36
NG_023270.1:g.4451G>T
NG_042828.1:g.9261G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015896.4:c.1248-1G>T MANE Select	NP_056980.2:n.1248-1G>T
ENST00000231749.8:c.1248-1G>T MANE Select	ENSP00000231749.3:n.1248-1G>T
NM_001308379.1:c.1233-1G>T	NP_001295308.1:n.1233-1G>T
NM_001308379.2:c.1233-1G>T	NP_001295308.1:n.1233-1G>T
NM_015896.2:c.1248-1G>T	NP_056980.2:n.1248-1G>T
NM_015896.3:c.1248-1G>T	NP_056980.2:n.1248-1G>T
ENST00000231749.7:c.1248-1G>T	ENSP00000231749.3:n.1248-1G>T
ENST00000360165.7:c.1233-1G>T	ENSP00000353289.3:n.1233-1G>T
ENST00000475688.1:n.1403-1G>T
ENST00000490675.5:n.301-1G>T
XM_005265216.2:c.1011-1G>T	XP_005265273.1:n.1011-1G>T
XM_005265216.3:c.1011-1G>T	XP_005265273.1:n.1011-1G>T