Canonical Allele Identifier: CA1577835

Gene: ZNF513

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27377947G>A , CM000664.2:g.27377947G>A	GRCh38
NC_000002.11:g.27600814G>A , CM000664.1:g.27600814G>A	GRCh37
NC_000002.10:g.27454318G>A	NCBI36
NG_028219.1:g.7798C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_144631.6:c.1224C>T MANE Select	NP_653232.3:p.Arg408=
ENST00000323703.11:c.1224C>T MANE Select	ENSP00000318373.6:p.Arg408=
NM_001201459.1:c.1038C>T	NP_001188388.1:p.Arg346=
NM_001201459.2:c.1038C>T	NP_001188388.1:p.Arg346=
NM_144631.5:c.1224C>T	NP_653232.3:p.Arg408=
ENST00000323703.10:c.1224C>T	ENSP00000318373.6:p.Arg408=
ENST00000407879.1:c.1038C>T	ENSP00000384874.1:p.Arg346=
ENST00000491924.1:n.343C>T
XM_005264142.1:c.1038C>T	XP_005264199.1:p.Arg346=
XM_005264142.2:c.1038C>T	XP_005264199.1:p.Arg346=
XM_005264143.2:c.720C>T	XP_005264200.1:p.Arg240=
XM_005264143.3:c.720C>T	XP_005264200.1:p.Arg240=