Canonical Allele Identifier: CA374408014

Gene: ZNF462

Linked Data

• MyVariant Identifiers: chr9:g.109690466G>C (hg19) ; chr9:g.106928185G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.106928185G>C , CM000671.2:g.106928185G>C	GRCh38
NC_000009.11:g.109690466G>C , CM000671.1:g.109690466G>C	GRCh37
NC_000009.10:g.108730287G>C	NCBI36
NG_052913.1:g.70089G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000277225.10:c.4273G>C MANE Select	ENSP00000277225.5:p.Gly1425Arg
ENST00000277225.9:c.4273G>C	ENSP00000277225.5:p.Gly1425Arg
ENST00000374686.6:c.922G>C	ENSP00000363818.2:p.Gly308Arg
ENST00000441147.6:c.808G>C	ENSP00000397306.2:p.Gly270Arg
ENST00000472574.1:c.281-2340G>C	ENSP00000476222.1:n.281-2340G>C
ENST00000480607.5:n.240+1021G>C
NM_021224.4:c.4273G>C	NP_067047.4:p.Gly1425Arg
XM_006717209.2:c.4273G>C	XP_006717272.1:p.Gly1425Arg
XM_006717210.2:c.4273G>C	XP_006717273.1:p.Gly1425Arg
XM_006717211.2:c.4273G>C	XP_006717274.1:p.Gly1425Arg
XM_006717212.2:c.4273G>C	XP_006717275.1:p.Gly1425Arg
XM_006717215.2:c.4273G>C	XP_006717278.1:p.Gly1425Arg
XM_006717216.2:c.4273G>C	XP_006717279.1:p.Gly1425Arg
XM_006717218.2:c.3252+1021G>C	XP_006717281.1:n.3252+1021G>C
XM_011518892.1:c.4273G>C	XP_011517194.1:p.Gly1425Arg
NM_001347997.1:c.3252+1021G>C	NP_001334926.1:n.3252+1021G>C
NM_021224.5:c.4273G>C	NP_067047.4:p.Gly1425Arg
XM_006717209.4:c.4273G>C	XP_006717272.1:p.Gly1425Arg
XM_006717211.4:c.4273G>C	XP_006717274.1:p.Gly1425Arg
XM_006717212.4:c.4273G>C	XP_006717275.1:p.Gly1425Arg
XM_006717215.4:c.4273G>C	XP_006717278.1:p.Gly1425Arg
XM_006717216.4:c.4273G>C	XP_006717279.1:p.Gly1425Arg
XM_006717218.4:c.3252+1021G>C	XP_006717281.1:n.3252+1021G>C
XM_017014996.2:c.4273G>C	XP_016870485.1:p.Gly1425Arg
XM_017014997.2:c.4273G>C	XP_016870486.1:p.Gly1425Arg
XM_017014998.2:c.3252+1021G>C	XP_016870487.1:n.3252+1021G>C
XM_024447629.1:c.4273G>C	XP_024303397.1:p.Gly1425Arg
NM_021224.6:c.4273G>C MANE Select	NP_067047.4:p.Gly1425Arg
NM_001347997.2:c.3252+1021G>C	NP_001334926.1:n.3252+1021G>C