Canonical Allele Identifier: CA1870356711

Gene: ZNF462

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.106870072G= , CM000671.2:g.106870072G=	GRCh38
NC_000009.11:g.109632353G= , CM000671.1:g.109632353G=	GRCh37
NC_000009.10:g.108672174G=	NCBI36
NG_052913.1:g.11976G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000277225.10:c.-31+6717G= MANE Select	ENSP00000277225.5:n.-31+6717G=
ENST00000277225.9:c.-31+6717G=	ENSP00000277225.5:n.-31+6717G=
ENST00000472574.1:c.-31+6717G=	ENSP00000476222.1:n.-31+6717G=
NM_021224.4:c.-31+6717G=	NP_067047.4:n.-31+6717G=
XM_006717209.2:c.-31+6717G=	XP_006717272.1:n.-31+6717G=
XM_006717210.2:c.-31+3881G=	XP_006717273.1:n.-31+3881G=
XM_006717212.2:c.-31+9859G=	XP_006717275.1:n.-31+9859G=
XM_006717215.2:c.-31+3881G=	XP_006717278.1:n.-31+3881G=
XM_006717216.2:c.-31+3881G=	XP_006717279.1:n.-31+3881G=
XM_006717218.2:c.-31+3881G=	XP_006717281.1:n.-31+3881G=
XM_011518892.1:c.-31+3881G=	XP_011517194.1:n.-31+3881G=
NM_001347997.1:c.-31+6717G=	NP_001334926.1:n.-31+6717G=
NM_021224.5:c.-31+6717G=	NP_067047.4:n.-31+6717G=
XM_006717209.4:c.-31+6717G=	XP_006717272.1:n.-31+6717G=
XM_006717212.4:c.-31+9859G=	XP_006717275.1:n.-31+9859G=
XM_006717215.4:c.-31+3881G=	XP_006717278.1:n.-31+3881G=
XM_006717216.4:c.-31+3881G=	XP_006717279.1:n.-31+3881G=
XM_006717218.4:c.-31+3881G=	XP_006717281.1:n.-31+3881G=
XM_017014996.2:c.-31+6041G=	XP_016870485.1:n.-31+6041G=
XM_017014998.2:c.-31+3881G=	XP_016870487.1:n.-31+3881G=
XM_024447629.1:c.-31+3881G=	XP_024303397.1:n.-31+3881G=
NM_021224.6:c.-31+6717G= MANE Select	NP_067047.4:n.-31+6717G=
NM_001347997.2:c.-31+6717G=	NP_001334926.1:n.-31+6717G=