Canonical Allele Identifier: CA5954663

Gene: ACCS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44083273C>T , CM000673.2:g.44083273C>T	GRCh38
NC_000011.9:g.44104823C>T , CM000673.1:g.44104823C>T	GRCh37
NC_000011.8:g.44061399C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263776.9:c.1216C>T MANE Select	ENSP00000263776.8:p.Arg406Cys
ENST00000263776.8:c.1216C>T	ENSP00000263776.8:p.Arg406Cys
ENST00000527346.5:n.2653C>T
ENST00000534035.1:n.295C>T
NM_001127219.1:c.1216C>T	NP_001120691.1:p.Arg406Cys
NM_032592.3:c.1216C>T	NP_115981.1:p.Arg406Cys
XM_005253170.2:c.1519C>T	XP_005253227.2:p.Arg507Cys
XM_005253172.2:c.826C>T	XP_005253229.1:p.Arg276Cys
XM_006718348.2:c.670C>T	XP_006718411.1:p.Arg224Cys
XM_011520406.1:c.1519C>T	XP_011518708.1:p.Arg507Cys
XM_011520407.1:c.853C>T	XP_011518709.1:p.Arg285Cys
XM_011520408.1:c.670C>T	XP_011518710.1:p.Arg224Cys
XM_011520409.1:c.511C>T	XP_011518711.1:p.Arg171Cys
XM_011520410.1:c.511C>T	XP_011518712.1:p.Arg171Cys
XR_930915.1:n.1922C>T
XM_005253170.3:c.1519C>T	XP_005253227.2:p.Arg507Cys
XM_011520406.2:c.1519C>T	XP_011518708.1:p.Arg507Cys
XM_011520410.2:c.511C>T	XP_011518712.1:p.Arg171Cys
XM_024448718.1:c.1216C>T	XP_024304486.1:p.Arg406Cys
XM_024448719.1:c.1216C>T	XP_024304487.1:p.Arg406Cys
XM_024448720.1:c.853C>T	XP_024304488.1:p.Arg285Cys
XM_024448721.1:c.670C>T	XP_024304489.1:p.Arg224Cys
XM_024448723.1:c.511C>T	XP_024304491.1:p.Arg171Cys
XR_001748003.1:n.2692C>T
XR_001748004.1:n.2999C>T
XR_001748006.1:n.2988C>T
XR_001748007.1:n.2955C>T
XR_930915.2:n.1923C>T
NM_001127219.2:c.1216C>T	NP_001120691.1:p.Arg406Cys
NM_032592.4:c.1216C>T MANE Select	NP_115981.1:p.Arg406Cys