Canonical Allele Identifier: CA1363902903

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342816_50342817delinsTG , CM000665.2:g.50342816_50342817delinsTG	GRCh38
NC_000003.11:g.50380247_50380248delinsTG , CM000665.1:g.50380247_50380248delinsTG	GRCh37
NC_000003.10:g.50355251_50355252delinsTG	NCBI36
NG_023270.1:g.3120_3121delinsCA
NG_042828.1:g.7930_7931delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+101_700+102delinsCA MANE Select	ENSP00000231749.3:n.700+101_700+102delinsCA
ENST00000231749.7:c.700+101_700+102delinsCA	ENSP00000231749.3:n.700+101_700+102delinsCA
ENST00000360165.7:c.600-162_600-161delinsCA	ENSP00000353289.3:n.600-162_600-161delinsCA
ENST00000442887.1:c.571+101_571+102delinsCA	ENSP00000393687.1:n.571+101_571+102delinsCA
ENST00000443080.5:c.*452+101_*452+102delinsCA	ENSP00000415661.1:n.*452+101_*452+102delinsCA
ENST00000475688.1:n.352_353delinsCA
NM_001308379.1:c.600-162_600-161delinsCA	NP_001295308.1:n.600-162_600-161delinsCA
NM_015896.2:c.700+101_700+102delinsCA	NP_056980.2:n.700+101_700+102delinsCA
NM_015896.3:c.700+101_700+102delinsCA	NP_056980.2:n.700+101_700+102delinsCA
XM_005265216.2:c.463+101_463+102delinsCA	XP_005265273.1:n.463+101_463+102delinsCA
XM_005265216.3:c.463+101_463+102delinsCA	XP_005265273.1:n.463+101_463+102delinsCA
NM_015896.4:c.700+101_700+102delinsCA MANE Select	NP_056980.2:n.700+101_700+102delinsCA
NM_001308379.2:c.600-162_600-161delinsCA	NP_001295308.1:n.600-162_600-161delinsCA