Canonical Allele Identifier: CA4367608

Gene: ZNF655

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99571720C>G , CM000669.2:g.99571720C>G	GRCh38
NC_000007.13:g.99169343C>G , CM000669.1:g.99169343C>G	GRCh37
NC_000007.12:g.99007279C>G	NCBI36
NG_029962.1:g.18299C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_138494.3:c.137-525C>G MANE Select	NP_612503.1:n.137-525C>G
ENST00000252713.9:c.137-525C>G MANE Select	ENSP00000252713.4:n.137-525C>G
NM_001009960.1:c.137-525C>G	NP_001009960.1:n.137-525C>G
NM_001083956.1:c.169C>G	NP_001077425.1:p.Gln57Glu
NM_001083956.2:c.169C>G	NP_001077425.1:p.Gln57Glu
NM_001085368.1:c.169C>G	NP_001078837.1:p.Gln57Glu
NM_001363332.1:c.169C>G	NP_001350261.1:p.Gln57Glu
NM_001363333.1:c.169C>G	NP_001350262.1:p.Gln57Glu
NM_001363334.1:c.137-525C>G	NP_001350263.1:n.137-525C>G
NM_138494.2:c.137-525C>G	NP_612503.1:n.137-525C>G
ENST00000252713.8:c.137-525C>G	ENSP00000252713.4:n.137-525C>G
ENST00000394163.2:c.137-525C>G	ENSP00000377718.2:n.137-525C>G
ENST00000412636.5:c.*148C>G	ENSP00000408555.1:n.*148C>G
ENST00000419215.2:n.65C>G
ENST00000422164.5:c.169C>G	ENSP00000389260.1:p.Gln57Glu
ENST00000422647.5:c.169C>G	ENSP00000393750.1:p.Gln57Glu
ENST00000424881.5:c.169C>G	ENSP00000393876.1:p.Gln57Glu
ENST00000425063.5:c.255C>G	ENSP00000392980.1:p.Pro85=
ENST00000427931.5:c.169C>G	ENSP00000392244.1:p.Gln57Glu
ENST00000454654.5:c.255C>G	ENSP00000403500.1:p.Pro85=
ENST00000455905.1:c.136+11025C>G	ENSP00000401282.1:n.136+11025C>G
ENST00000486324.2:n.256+11025C>G
ENST00000493277.5:c.169C>G	ENSP00000419135.1:p.Gln57Glu
ENST00000494357.1:n.1522C>G
ENST00000626122.2:c.255C>G	ENSP00000486262.1:p.Pro85=
XM_017012607.2:c.137-525C>G	XP_016868096.1:n.137-525C>G
XM_017012611.2:c.382C>G	XP_016868100.1:p.Gln128Glu