Canonical Allele Identifier: CA5548982

Gene: ASCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72161537C>T , CM000672.2:g.72161537C>T	GRCh38
NC_000010.10:g.73921295C>T , CM000672.1:g.73921295C>T	GRCh37
NC_000010.9:g.73591301C>T	NCBI36
NG_031890.1:g.60598G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001198800.3:c.626+1G>A MANE Select	NP_001185729.1:n.626+1G>A
ENST00000672957.1:c.626+1G>A MANE Select	ENSP00000500935.1:n.626+1G>A
NM_001198798.2:c.626+1G>A	NP_001185727.1:n.626+1G>A
NM_001198799.2:c.710+1G>A	NP_001185728.1:n.710+1G>A
NM_001198799.3:c.710+1G>A	NP_001185728.1:n.710+1G>A
NM_001198800.2:c.626+1G>A	NP_001185729.1:n.626+1G>A
NM_001369085.1:c.692+1G>A	NP_001356014.1:n.692+1G>A
NM_001369086.1:c.692+1G>A	NP_001356015.1:n.692+1G>A
NM_001369087.1:c.626+1G>A	NP_001356016.1:n.626+1G>A
NM_001369088.1:c.626+1G>A	NP_001356017.1:n.626+1G>A
NM_001369089.1:c.626+1G>A	NP_001356018.1:n.626+1G>A
NM_001369090.1:c.626+1G>A	NP_001356019.1:n.626+1G>A
NM_001369091.1:c.626+1G>A	NP_001356020.1:n.626+1G>A
NM_001369092.1:c.626+1G>A	NP_001356021.1:n.626+1G>A
NM_001369093.1:c.626+1G>A	NP_001356022.1:n.626+1G>A
NM_001369094.1:c.626+1G>A	NP_001356023.1:n.626+1G>A
NM_001369095.1:c.626+1G>A	NP_001356024.1:n.626+1G>A
NM_001369096.1:c.626+1G>A	NP_001356025.1:n.626+1G>A
NM_001369097.1:c.626+1G>A	NP_001356026.1:n.626+1G>A
NM_001369098.1:c.626+1G>A	NP_001356027.1:n.626+1G>A
NM_001369099.1:c.692+1G>A	NP_001356028.1:n.692+1G>A
NM_001369100.1:c.626+1G>A	NP_001356029.1:n.626+1G>A
NM_001369101.1:c.509+1G>A	NP_001356030.1:n.509+1G>A
NM_001369102.1:c.509+1G>A	NP_001356031.1:n.509+1G>A
NM_001369103.1:c.626+1G>A	NP_001356032.1:n.626+1G>A
NM_001369104.1:c.626+1G>A	NP_001356033.1:n.626+1G>A
NM_001369105.1:c.509+1G>A	NP_001356034.1:n.509+1G>A
NM_001369106.1:c.509+1G>A	NP_001356035.1:n.509+1G>A
NM_001369107.1:c.509+1G>A	NP_001356036.1:n.509+1G>A
NM_001369108.1:c.626+1G>A	NP_001356037.1:n.626+1G>A
NM_001369109.1:c.626+1G>A	NP_001356038.1:n.626+1G>A
NM_001369110.1:c.626+1G>A	NP_001356039.1:n.626+1G>A
NM_001369111.1:c.626+1G>A	NP_001356040.1:n.626+1G>A
NM_001369112.1:c.626+1G>A	NP_001356041.1:n.626+1G>A
NR_045564.1:n.973+1G>A
ENST00000317126.8:c.626+1G>A	ENSP00000320461.4:n.626+1G>A
ENST00000317168.10:c.626+1G>A	ENSP00000320810.6:n.626+1G>A
ENST00000317168.11:c.626+1G>A	ENSP00000320810.7:n.626+1G>A
ENST00000342444.8:c.710+1G>A	ENSP00000339404.4:n.710+1G>A
ENST00000394915.7:c.710+1G>A	ENSP00000378373.3:n.710+1G>A
ENST00000394919.5:c.626+1G>A	ENSP00000378377.1:n.626+1G>A
ENST00000486689.6:c.420+1G>A
ENST00000525286.5:c.316+1G>A
ENST00000525286.6:c.316+1G>A
ENST00000530394.5:c.19+1G>A
ENST00000671788.1:c.626+1G>A	ENSP00000500906.1:n.626+1G>A
ENST00000672121.1:c.413+1G>A	ENSP00000500771.1:n.413+1G>A
ENST00000672774.1:c.686+1G>A	ENSP00000500488.1:n.686+1G>A
ENST00000672809.1:n.177+1G>A
ENST00000672940.1:c.626+1G>A	ENSP00000500074.1:n.626+1G>A
ENST00000673599.1:c.*532+1G>A	ENSP00000499820.1:n.*532+1G>A
XM_006717873.2:c.626+1G>A	XP_006717936.1:n.626+1G>A
XM_006717873.4:c.626+1G>A	XP_006717936.1:n.626+1G>A
XM_011539840.1:c.626+1G>A	XP_011538142.1:n.626+1G>A
XM_011539841.1:c.626+1G>A	XP_011538143.1:n.626+1G>A
XM_011539841.3:c.626+1G>A	XP_011538143.1:n.626+1G>A
XM_011539842.1:c.626+1G>A	XP_011538144.1:n.626+1G>A
XM_011539842.3:c.626+1G>A	XP_011538144.1:n.626+1G>A
XM_011539843.1:c.626+1G>A	XP_011538145.1:n.626+1G>A
XM_011539844.1:c.626+1G>A	XP_011538146.1:n.626+1G>A
XM_017016291.2:c.626+1G>A	XP_016871780.1:n.626+1G>A
XM_017016292.2:c.626+1G>A	XP_016871781.1:n.626+1G>A
XM_017016293.2:c.626+1G>A	XP_016871782.1:n.626+1G>A
XM_017016294.2:c.626+1G>A	XP_016871783.1:n.626+1G>A
XM_024448030.1:c.692+1G>A	XP_024303798.1:n.692+1G>A
XM_024448031.1:c.692+1G>A	XP_024303799.1:n.692+1G>A
XM_024448032.1:c.692+1G>A	XP_024303800.1:n.692+1G>A