Canonical Allele Identifier: CA1577904
Community Standard Title: NM_144631.6(ZNF513):c.900C>T (p.Cys300=)
Gene: ZNF513 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27378271G>A , CM000664.2:g.27378271G>A GRCh38
NC_000002.11:g.27601138G>A , CM000664.1:g.27601138G>A GRCh37
NC_000002.10:g.27454642G>A NCBI36
NG_028219.1:g.7474C>T

Transcript Alleles

HGVS Amino-acid Change
NM_144631.6:c.900C>T MANE Select NP_653232.3:p.Cys300=
ENST00000323703.11:c.900C>T MANE Select ENSP00000318373.6:p.Cys300=
NM_001201459.1:c.714C>T NP_001188388.1:p.Cys238=
NM_001201459.2:c.714C>T NP_001188388.1:p.Cys238=
NM_144631.5:c.900C>T NP_653232.3:p.Cys300=
ENST00000323703.10:c.900C>T ENSP00000318373.6:p.Cys300=
ENST00000407879.1:c.714C>T ENSP00000384874.1:p.Cys238=
ENST00000491924.1:n.259+196C>T
XM_005264142.1:c.714C>T XP_005264199.1:p.Cys238=
XM_005264142.2:c.714C>T XP_005264199.1:p.Cys238=
XM_005264143.2:c.396C>T XP_005264200.1:p.Cys132=
XM_005264143.3:c.396C>T XP_005264200.1:p.Cys132=