Canonical Allele Identifier: CA377398204

Gene: ADK

Linked Data

• MyVariant Identifiers: chr10:g.76285186T>C (hg19) ; chr10:g.74525428T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74525428T>C , CM000672.2:g.74525428T>C	GRCh38
NC_000010.10:g.76285186T>C , CM000672.1:g.76285186T>C	GRCh37
NC_000010.9:g.75955192T>C	NCBI36
NG_030484.1:g.379244T>C
NG_030484.2:g.379244T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286621.7:c.726+2T>C	ENSP00000286621.3:n.726+2T>C
ENST00000372734.5:c.675+2T>C	ENSP00000361819.3:n.675+2T>C
ENST00000539909.6:c.726+2T>C MANE Select	ENSP00000443965.2:n.726+2T>C
ENST00000541550.6:c.675+2T>C	ENSP00000438321.2:n.675+2T>C
ENST00000672394.1:c.450+2T>C	ENSP00000500390.1:n.450+2T>C
ENST00000672429.1:c.556-63854T>C	ENSP00000500292.1:n.556-63854T>C
ENST00000672604.1:c.466+2T>C
ENST00000672920.1:c.*471+2T>C	ENSP00000500141.1:n.*471+2T>C
ENST00000673027.1:c.621+2T>C	ENSP00000500201.1:n.621+2T>C
ENST00000673310.1:c.675+2T>C	ENSP00000500097.1:n.675+2T>C
ENST00000673352.1:c.726+2T>C	ENSP00000500056.1:n.726+2T>C
ENST00000286621.6:c.726+2T>C	ENSP00000286621.2:n.726+2T>C
ENST00000372734.3:c.675+2T>C	ENSP00000361819.3:n.675+2T>C
ENST00000467840.1:n.63+2T>C
ENST00000539909.5:c.556-63854T>C	ENSP00000443965.1:n.556-63854T>C
ENST00000541550.5:c.621+2T>C	ENSP00000438321.1:n.621+2T>C
NM_001123.3:c.675+2T>C	NP_001114.2:n.675+2T>C
NM_001202449.1:c.621+2T>C	NP_001189378.1:n.621+2T>C
NM_001202450.1:c.556-63854T>C	NP_001189379.1:n.556-63854T>C
NM_006721.3:c.726+2T>C	NP_006712.2:n.726+2T>C
NR_120673.1:n.259+2338A>G
XM_011539297.1:c.642+2T>C	XP_011537599.1:n.642+2T>C
XM_017015698.1:c.726+2T>C	XP_016871187.1:n.726+2T>C
XM_017015699.1:c.531+2T>C	XP_016871188.1:n.531+2T>C
XM_017015700.1:c.726+2T>C	XP_016871189.1:n.726+2T>C
XM_017015701.1:c.505-63854T>C	XP_016871190.1:n.505-63854T>C
XM_017015702.1:c.675+2T>C	XP_016871191.1:n.675+2T>C
XM_017015703.2:c.450+2T>C	XP_016871192.1:n.450+2T>C
XM_017015704.1:c.726+2T>C	XP_016871193.1:n.726+2T>C
XM_017015705.1:c.556-63854T>C	XP_016871194.1:n.556-63854T>C
XM_017015706.1:c.675+2T>C	XP_016871195.1:n.675+2T>C
NM_001369123.1:c.726+2T>C	NP_001356052.1:n.726+2T>C
NM_001369124.1:c.505-63854T>C	NP_001356053.1:n.505-63854T>C
NM_006721.4:c.726+2T>C MANE Select	NP_006712.2:n.726+2T>C
NM_001123.4:c.675+2T>C	NP_001114.2:n.675+2T>C
NM_001202449.2:c.621+2T>C	NP_001189378.1:n.621+2T>C
NM_001202450.2:c.556-63854T>C	NP_001189379.1:n.556-63854T>C