Canonical Allele Identifier: CA354293774

Gene: ZNF148

Linked Data

• MyVariant Identifiers: chr3:g.124951491C>A (hg19) ; chr3:g.125232647C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.125232647C>A , CM000665.2:g.125232647C>A	GRCh38
NC_000003.11:g.124951491C>A , CM000665.1:g.124951491C>A	GRCh37
NC_000003.10:g.126434181C>A	NCBI36
NG_052987.1:g.147708G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471196.2:c.2079G>T	ENSP00000420038.2:p.Glu693Asp
ENST00000700044.1:c.2079G>T	ENSP00000514760.1:p.Glu693Asp
ENST00000360647.9:c.2079G>T MANE Select	ENSP00000353863.4:p.Glu693Asp
ENST00000360647.8:c.2079G>T	ENSP00000353863.4:p.Glu693Asp
ENST00000468369.5:c.129G>T	ENSP00000420102.1:p.Glu43Asp
ENST00000484491.5:c.2079G>T	ENSP00000420335.1:p.Glu693Asp
ENST00000485866.5:c.2079G>T	ENSP00000420448.1:p.Glu693Asp
ENST00000492394.5:c.2079G>T	ENSP00000419322.1:p.Glu693Asp
ENST00000496732.1:n.181G>T
ENST00000497929.1:n.2075G>T
NM_021964.2:c.2079G>T	NP_068799.2:p.Glu693Asp
NM_001348424.1:c.2079G>T	NP_001335353.1:p.Glu693Asp
NM_001348425.2:c.2079G>T	NP_001335354.1:p.Glu693Asp
NM_001348426.2:c.2079G>T	NP_001335355.1:p.Glu693Asp
NM_001348427.2:c.2079G>T	NP_001335356.1:p.Glu693Asp
NM_001348428.2:c.2079G>T	NP_001335357.1:p.Glu693Asp
NM_001348429.2:c.2079G>T	NP_001335358.1:p.Glu693Asp
NM_001348430.2:c.2079G>T	NP_001335359.1:p.Glu693Asp
NM_001348431.2:c.2079G>T	NP_001335360.1:p.Glu693Asp
NM_001348432.2:c.2079G>T	NP_001335361.1:p.Glu693Asp
NM_001348433.2:c.2079G>T	NP_001335362.1:p.Glu693Asp
NM_001348434.2:c.1953G>T	NP_001335363.1:p.Glu651Asp
NM_021964.3:c.2079G>T MANE Select	NP_068799.2:p.Glu693Asp