Canonical Allele Identifier: CA377398175

Gene: ADK

Linked Data

• gnomAD v4: 10-74525416-G-A
• MyVariant Identifiers: chr10:g.76285174G>A (hg19) ; chr10:g.74525416G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74525416G>A , CM000672.2:g.74525416G>A	GRCh38
NC_000010.10:g.76285174G>A , CM000672.1:g.76285174G>A	GRCh37
NC_000010.9:g.75955180G>A	NCBI36
NG_030484.1:g.379232G>A
NG_030484.2:g.379232G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000286621.7:c.716G>A	ENSP00000286621.3:p.Gly239Glu
ENST00000372734.5:c.665G>A	ENSP00000361819.3:p.Gly222Glu
ENST00000539909.6:c.716G>A MANE Select	ENSP00000443965.2:p.Gly239Glu
ENST00000541550.6:c.665G>A	ENSP00000438321.2:p.Gly222Glu
ENST00000672394.1:c.440G>A	ENSP00000500390.1:p.Gly147Glu
ENST00000672429.1:c.556-63866G>A	ENSP00000500292.1:n.556-63866G>A
ENST00000672604.1:c.456G>A
ENST00000672920.1:c.*461G>A	ENSP00000500141.1:n.*461G>A
ENST00000673027.1:c.611G>A	ENSP00000500201.1:p.Gly204Glu
ENST00000673310.1:c.665G>A	ENSP00000500097.1:p.Gly222Glu
ENST00000673352.1:c.716G>A	ENSP00000500056.1:p.Gly239Glu
ENST00000286621.6:c.716G>A	ENSP00000286621.2:p.Gly239Glu
ENST00000372734.3:c.665G>A	ENSP00000361819.3:p.Gly222Glu
ENST00000467840.1:n.53G>A
ENST00000539909.5:c.556-63866G>A	ENSP00000443965.1:n.556-63866G>A
ENST00000541550.5:c.611G>A	ENSP00000438321.1:p.Gly204Glu
NM_001123.3:c.665G>A	NP_001114.2:p.Gly222Glu
NM_001202449.1:c.611G>A	NP_001189378.1:p.Gly204Glu
NM_001202450.1:c.556-63866G>A	NP_001189379.1:n.556-63866G>A
NM_006721.3:c.716G>A	NP_006712.2:p.Gly239Glu
NR_120673.1:n.259+2350C>T
XM_011539297.1:c.632G>A	XP_011537599.1:p.Gly211Glu
XM_017015698.1:c.716G>A	XP_016871187.1:p.Gly239Glu
XM_017015699.1:c.521G>A	XP_016871188.1:p.Gly174Glu
XM_017015700.1:c.716G>A	XP_016871189.1:p.Gly239Glu
XM_017015701.1:c.505-63866G>A	XP_016871190.1:n.505-63866G>A
XM_017015702.1:c.665G>A	XP_016871191.1:p.Gly222Glu
XM_017015703.2:c.440G>A	XP_016871192.1:p.Gly147Glu
XM_017015704.1:c.716G>A	XP_016871193.1:p.Gly239Glu
XM_017015705.1:c.556-63866G>A	XP_016871194.1:n.556-63866G>A
XM_017015706.1:c.665G>A	XP_016871195.1:p.Gly222Glu
NM_001369123.1:c.716G>A	NP_001356052.1:p.Gly239Glu
NM_001369124.1:c.505-63866G>A	NP_001356053.1:n.505-63866G>A
NM_006721.4:c.716G>A MANE Select	NP_006712.2:p.Gly239Glu
NM_001123.4:c.665G>A	NP_001114.2:p.Gly222Glu
NM_001202449.2:c.611G>A	NP_001189378.1:p.Gly204Glu
NM_001202450.2:c.556-63866G>A	NP_001189379.1:n.556-63866G>A