Canonical Allele Identifier: CA3913820

Gene: ZNF292

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87254835G>A , CM000668.2:g.87254835G>A	GRCh38
NC_000006.11:g.87964553G>A , CM000668.1:g.87964553G>A	GRCh37
NC_000006.10:g.88021272G>A	NCBI36
NG_054887.1:g.104285G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015021.3:c.1206G>A MANE Select	NP_055836.1:p.Ala402=
ENST00000369577.8:c.1206G>A MANE Select	ENSP00000358590.3:p.Ala402=
NM_001351444.1:c.786G>A	NP_001338373.1:p.Ala262=
NM_001351444.2:c.786G>A	NP_001338373.1:p.Ala262=
NM_015021.1:c.1206G>A	NP_055836.1:p.Ala402=
NM_015021.2:c.1206G>A	NP_055836.1:p.Ala402=
ENST00000339907.8:c.1191G>A	ENSP00000342847.4:p.Ala397=
ENST00000369577.7:c.1206G>A	ENSP00000358590.3:p.Ala402=
ENST00000466062.2:c.624G>A
ENST00000466062.3:c.1248G>A
ENST00000496806.2:c.200-5240G>A	ENSP00000428857.1:n.200-5240G>A
ENST00000699914.1:c.1206G>A	ENSP00000514683.1:p.Ala402=
ENST00000699923.1:c.1203G>A	ENSP00000514690.1:p.Ala401=
ENST00000699925.1:c.*1153G>A	ENSP00000514691.1:n.*1153G>A
ENST00000699989.1:n.4666G>A
ENST00000699991.1:c.424G>A
XM_005248697.3:c.786G>A	XP_005248754.1:p.Ala262=
XM_005248697.4:c.786G>A	XP_005248754.1:p.Ala262=
XM_005248698.3:c.432G>A	XP_005248755.1:p.Ala144=
XM_011535625.1:c.240G>A	XP_011533927.1:p.Ala80=
XM_011535625.2:c.240G>A	XP_011533927.1:p.Ala80=
XM_017010576.1:c.786G>A	XP_016866065.1:p.Ala262=
XM_017010577.1:c.786G>A	XP_016866066.1:p.Ala262=
XM_017010578.2:c.786G>A	XP_016866067.1:p.Ala262=
XM_017010579.1:c.786G>A	XP_016866068.1:p.Ala262=
XM_017010580.1:c.786G>A	XP_016866069.1:p.Ala262=
XM_017010582.1:c.786G>A	XP_016866071.1:p.Ala262=
XM_017010583.1:c.786G>A	XP_016866072.1:p.Ala262=
XM_017010584.2:c.786G>A	XP_016866073.1:p.Ala262=