Canonical Allele Identifier: CA1870387278

Gene: ZNF462

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.106928016C= , CM000671.2:g.106928016C=	GRCh38
NC_000009.11:g.109690297C= , CM000671.1:g.109690297C=	GRCh37
NC_000009.10:g.108730118C=	NCBI36
NG_052913.1:g.69920C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000277225.10:c.4104C= MANE Select	ENSP00000277225.5:p.Thr1368=
ENST00000277225.9:c.4104C=	ENSP00000277225.5:p.Thr1368=
ENST00000374686.6:c.753C=	ENSP00000363818.2:p.Thr251=
ENST00000441147.6:c.639C=	ENSP00000397306.2:p.Thr213=
ENST00000472574.1:c.281-2509C=	ENSP00000476222.1:n.281-2509C=
ENST00000480607.5:n.240+852C=
NM_021224.4:c.4104C=	NP_067047.4:p.Thr1368=
XM_006717209.2:c.4104C=	XP_006717272.1:p.Thr1368=
XM_006717210.2:c.4104C=	XP_006717273.1:p.Thr1368=
XM_006717211.2:c.4104C=	XP_006717274.1:p.Thr1368=
XM_006717212.2:c.4104C=	XP_006717275.1:p.Thr1368=
XM_006717215.2:c.4104C=	XP_006717278.1:p.Thr1368=
XM_006717216.2:c.4104C=	XP_006717279.1:p.Thr1368=
XM_006717218.2:c.3252+852C=	XP_006717281.1:n.3252+852C=
XM_011518892.1:c.4104C=	XP_011517194.1:p.Thr1368=
NM_001347997.1:c.3252+852C=	NP_001334926.1:n.3252+852C=
NM_021224.5:c.4104C=	NP_067047.4:p.Thr1368=
XM_006717209.4:c.4104C=	XP_006717272.1:p.Thr1368=
XM_006717211.4:c.4104C=	XP_006717274.1:p.Thr1368=
XM_006717212.4:c.4104C=	XP_006717275.1:p.Thr1368=
XM_006717215.4:c.4104C=	XP_006717278.1:p.Thr1368=
XM_006717216.4:c.4104C=	XP_006717279.1:p.Thr1368=
XM_006717218.4:c.3252+852C=	XP_006717281.1:n.3252+852C=
XM_017014996.2:c.4104C=	XP_016870485.1:p.Thr1368=
XM_017014997.2:c.4104C=	XP_016870486.1:p.Thr1368=
XM_017014998.2:c.3252+852C=	XP_016870487.1:n.3252+852C=
XM_024447629.1:c.4104C=	XP_024303397.1:p.Thr1368=
NM_021224.6:c.4104C= MANE Select	NP_067047.4:p.Thr1368=
NM_001347997.2:c.3252+852C=	NP_001334926.1:n.3252+852C=