Canonical Allele Identifier: CA5564039

Gene: ADK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74589271T>C , CM000672.2:g.74589271T>C	GRCh38
NC_000010.10:g.76349029T>C , CM000672.1:g.76349029T>C	GRCh37
NC_000010.9:g.76019035T>C	NCBI36
NG_030484.1:g.443087T>C
NG_030484.2:g.443087T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286621.7:c.727-11T>C	ENSP00000286621.3:n.727-11T>C
ENST00000372734.5:c.676-11T>C	ENSP00000361819.3:n.676-11T>C
ENST00000539909.6:c.727-11T>C MANE Select	ENSP00000443965.2:n.727-11T>C
ENST00000541550.6:c.676-11T>C	ENSP00000438321.2:n.676-11T>C
ENST00000672394.1:c.451-11T>C	ENSP00000500390.1:n.451-11T>C
ENST00000672429.1:c.556-11T>C	ENSP00000500292.1:n.556-11T>C
ENST00000672604.1:c.467-11T>C
ENST00000672920.1:c.*472-11T>C	ENSP00000500141.1:n.*472-11T>C
ENST00000673027.1:c.622-11T>C	ENSP00000500201.1:n.622-11T>C
ENST00000673310.1:c.*320-11T>C	ENSP00000500097.1:n.*320-11T>C
ENST00000673352.1:c.727-11T>C	ENSP00000500056.1:n.727-11T>C
ENST00000286621.6:c.727-11T>C	ENSP00000286621.2:n.727-11T>C
ENST00000372734.3:c.676-11T>C	ENSP00000361819.3:n.676-11T>C
ENST00000539909.5:c.556-11T>C	ENSP00000443965.1:n.556-11T>C
ENST00000541550.5:c.622-11T>C	ENSP00000438321.1:n.622-11T>C
NM_001123.3:c.676-11T>C	NP_001114.2:n.676-11T>C
NM_001202449.1:c.622-11T>C	NP_001189378.1:n.622-11T>C
NM_001202450.1:c.556-11T>C	NP_001189379.1:n.556-11T>C
NM_006721.3:c.727-11T>C	NP_006712.2:n.727-11T>C
XM_011539297.1:c.643-11T>C	XP_011537599.1:n.643-11T>C
XM_017015698.1:c.727-11T>C	XP_016871187.1:n.727-11T>C
XM_017015699.1:c.532-11T>C	XP_016871188.1:n.532-11T>C
XM_017015700.1:c.727-11T>C	XP_016871189.1:n.727-11T>C
XM_017015701.1:c.505-11T>C	XP_016871190.1:n.505-11T>C
XM_017015702.1:c.676-11T>C	XP_016871191.1:n.676-11T>C
XM_017015703.2:c.451-11T>C	XP_016871192.1:n.451-11T>C
XM_017015705.1:c.556-11T>C	XP_016871194.1:n.556-11T>C
NM_001369123.1:c.727-11T>C	NP_001356052.1:n.727-11T>C
NM_001369124.1:c.505-11T>C	NP_001356053.1:n.505-11T>C
NM_006721.4:c.727-11T>C MANE Select	NP_006712.2:n.727-11T>C
NM_001123.4:c.676-11T>C	NP_001114.2:n.676-11T>C
NM_001202449.2:c.622-11T>C	NP_001189378.1:n.622-11T>C
NM_001202450.2:c.556-11T>C	NP_001189379.1:n.556-11T>C