Canonical Allele Identifier: CA13136150

Gene: ZNF462

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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