Canonical Allele Identifier: CA2478336870

Gene: ZNF644

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.90916786G= , CM000663.2:g.90916786G=	GRCh38
NC_000001.10:g.91382343G= , CM000663.1:g.91382343G=	GRCh37
NC_000001.9:g.91154931G=	NCBI36
NG_029760.1:g.110470C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337393.10:c.*12C= MANE Select	ENSP00000337008.5:n.*12C=
ENST00000337393.9:c.*12C=	ENSP00000337008.5:n.*12C=
ENST00000347275.9:c.*12C=	ENSP00000340828.5:n.*12C=
ENST00000361321.5:c.*12C=	ENSP00000354659.5:n.*12C=
ENST00000370440.5:c.*12C=	ENSP00000359469.1:n.*12C=
ENST00000467231.5:n.455C=
ENST00000479798.1:n.429C=
NM_016620.3:c.*12C=	NP_057704.2:n.*12C=
NM_032186.4:c.*12C=	NP_115562.3:n.*12C=
NM_201269.2:c.*12C=	NP_958357.1:n.*12C=
XM_005271257.3:c.*12C=	XP_005271314.1:n.*12C=
XM_005271260.3:c.*12C=	XP_005271317.1:n.*12C=
XM_011542258.1:c.*12C=	XP_011540560.1:n.*12C=
XM_011542259.1:c.*12C=	XP_011540561.1:n.*12C=
XM_011542260.1:c.*12C=	XP_011540562.1:n.*12C=
XM_011542261.1:c.*12C=	XP_011540563.1:n.*12C=
XM_005271257.5:c.*12C=	XP_005271314.1:n.*12C=
XM_005271260.5:c.*12C=	XP_005271317.1:n.*12C=
XM_011542258.3:c.*12C=	XP_011540560.1:n.*12C=
XM_011542259.3:c.*12C=	XP_011540561.1:n.*12C=
XM_011542260.3:c.*12C=	XP_011540562.1:n.*12C=
XM_011542261.3:c.*12C=	XP_011540563.1:n.*12C=
XM_017002487.2:c.*12C=	XP_016857976.1:n.*12C=
XM_017002488.2:c.*12C=	XP_016857977.1:n.*12C=
XM_017002489.2:c.*12C=	XP_016857978.1:n.*12C=
XM_017002490.2:c.*12C=	XP_016857979.1:n.*12C=
XM_017002491.2:c.*12C=	XP_016857980.1:n.*12C=
XM_017002492.2:c.*12C=	XP_016857981.1:n.*12C=
XM_017002493.2:c.*12C=	XP_016857982.1:n.*12C=
XM_017002494.1:c.*12C=	XP_016857983.1:n.*12C=
NM_201269.3:c.*12C= MANE Select	NP_958357.1:n.*12C=
NM_016620.4:c.*12C=	NP_057704.2:n.*12C=
NM_032186.5:c.*12C=	NP_115562.3:n.*12C=