Canonical Allele Identifier: CA352941546

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380348C>G (hg19) ; chr3:g.50342917C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342917C>G , CM000665.2:g.50342917C>G	GRCh38
NC_000003.11:g.50380348C>G , CM000665.1:g.50380348C>G	GRCh37
NC_000003.10:g.50355352C>G	NCBI36
NG_023270.1:g.3020G>C
NG_042828.1:g.7830G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+1G>C MANE Select	ENSP00000231749.3:n.700+1G>C
ENST00000231749.7:c.700+1G>C	ENSP00000231749.3:n.700+1G>C
ENST00000360165.7:c.599+201G>C	ENSP00000353289.3:n.599+201G>C
ENST00000442887.1:c.571+1G>C	ENSP00000393687.1:n.571+1G>C
ENST00000443080.5:c.*452+1G>C	ENSP00000415661.1:n.*452+1G>C
ENST00000475688.1:n.252G>C
NM_001308379.1:c.599+201G>C	NP_001295308.1:n.599+201G>C
NM_015896.2:c.700+1G>C	NP_056980.2:n.700+1G>C
NM_015896.3:c.700+1G>C	NP_056980.2:n.700+1G>C
XM_005265216.2:c.463+1G>C	XP_005265273.1:n.463+1G>C
XM_005265216.3:c.463+1G>C	XP_005265273.1:n.463+1G>C
NM_015896.4:c.700+1G>C MANE Select	NP_056980.2:n.700+1G>C
NM_001308379.2:c.599+201G>C	NP_001295308.1:n.599+201G>C