Canonical Allele Identifier: CA9500671

Gene: ZNF229

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44429731T>A , CM000681.2:g.44429731T>A	GRCh38
NC_000019.9:g.44933906T>A , CM000681.1:g.44933906T>A	GRCh37
NC_000019.8:g.49625746T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014518.4:c.1050A>T MANE Select	NP_055333.3:p.Arg350Ser
ENST00000614049.5:c.1050A>T MANE Select	ENSP00000479884.1:p.Arg350Ser
NM_001278510.2:c.1032A>T	NP_001265439.2:p.Arg344Ser
NM_001278510.3:c.1032A>T	NP_001265439.2:p.Arg344Ser
NM_014518.3:c.1050A>T	NP_055333.3:p.Arg350Ser
NR_103551.2:n.1939A>T
NR_103551.3:n.1934A>T
ENST00000591289.5:n.523-12185A>T
ENST00000613197.4:c.1032A>T	ENSP00000479807.1:p.Arg344Ser
ENST00000614049.4:c.1050A>T	ENSP00000479884.1:p.Arg350Ser
ENST00000620012.4:c.*1253A>T	ENSP00000483138.1:n.*1253A>T
XM_006723372.2:c.966A>T	XP_006723435.1:p.Arg322Ser
XM_006723372.4:c.966A>T	XP_006723435.1:p.Arg322Ser
XM_011527292.1:c.1032A>T	XP_011525594.1:p.Arg344Ser
XM_011527292.2:c.1032A>T	XP_011525594.1:p.Arg344Ser
XM_017027280.2:c.12A>T	XP_016882769.1:p.Arg4Ser