Canonical Allele Identifier: CA912996172

Gene: ACD

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67659528A>T , CM000678.2:g.67659528A>T	GRCh38
NC_000016.9:g.67693431A>T , CM000678.1:g.67693431A>T	GRCh37
NC_000016.8:g.66250932A>T	NCBI36
NG_042874.1:g.6288T>A
NG_054728.1:g.19610A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001082486.2:c.413+9T>A MANE Select	NP_001075955.2:n.413+9T>A
ENST00000620761.6:c.413+9T>A MANE Select	ENSP00000478084.1:n.413+9T>A
NM_001082486.1:c.671+9T>A	NP_001075955.1:n.671+9T>A
NM_001082487.1:c.662+9T>A	NP_001075956.1:n.662+9T>A
NM_022914.2:c.662+9T>A	NP_075065.2:n.662+9T>A
NM_022914.3:c.404+9T>A	NP_075065.3:n.404+9T>A
ENST00000219251.12:c.662+9T>A	ENSP00000219251.7:n.662+9T>A
ENST00000219251.13:c.404+9T>A	ENSP00000219251.8:n.404+9T>A
ENST00000393919.8:c.671+9T>A	ENSP00000377496.4:n.671+9T>A
ENST00000602320.1:c.404+9T>A	ENSP00000473679.2:n.404+9T>A
ENST00000602382.6:c.413+9T>A	ENSP00000473313.2:n.413+9T>A
ENST00000602423.1:n.323T>A
ENST00000602519.1:n.522T>A
ENST00000602519.2:n.535T>A
ENST00000602622.5:n.663T>A
ENST00000602780.2:n.669T>A
ENST00000602850.5:c.244+9T>A	ENSP00000473595.2:n.244+9T>A
ENST00000602850.6:c.*193+9T>A	ENSP00000473595.3:n.*193+9T>A
ENST00000602860.5:n.483T>A
ENST00000602860.6:n.965T>A
ENST00000602945.5:n.483+9T>A
ENST00000602945.6:n.555+9T>A
ENST00000620338.4:c.671+9T>A	ENSP00000483117.1:n.671+9T>A
ENST00000620761.4:c.413+9T>A	ENSP00000478084.1:n.413+9T>A
ENST00000695641.1:n.962T>A
ENST00000695648.1:c.395+9T>A	ENSP00000512081.1:n.395+9T>A
ENST00000695649.1:n.1038T>A
ENST00000695650.1:c.*175+9T>A	ENSP00000512082.1:n.*175+9T>A
ENST00000695656.1:n.492T>A
ENST00000695657.1:n.450T>A
ENST00000695658.1:c.413+9T>A	ENSP00000512088.1:n.413+9T>A
ENST00000695659.1:c.413+9T>A	ENSP00000512089.1:n.413+9T>A
ENST00000695660.1:n.558T>A
ENST00000695661.1:c.404+9T>A	ENSP00000512090.1:n.404+9T>A
ENST00000695662.1:c.413+9T>A	ENSP00000512091.1:n.413+9T>A
ENST00000695694.1:c.413+9T>A	ENSP00000512105.1:n.413+9T>A
ENST00000695695.1:n.559+9T>A
ENST00000695696.1:n.426T>A
ENST00000695697.1:c.413+9T>A	ENSP00000512106.1:n.413+9T>A
ENST00000695698.1:n.444T>A
ENST00000695699.1:n.441+9T>A
ENST00000695700.1:n.410T>A
ENST00000695701.1:n.428T>A
ENST00000695702.1:n.160T>A
ENST00000695710.1:n.298T>A
ENST00000695711.1:c.413+9T>A	ENSP00000512109.1:n.413+9T>A
ENST00000695712.1:c.*163+9T>A	ENSP00000512110.1:n.*163+9T>A
ENST00000695713.1:c.77+9T>A	ENSP00000512111.1:n.77+9T>A
ENST00000695732.1:c.413+9T>A	ENSP00000512125.1:n.413+9T>A
ENST00000695733.1:c.413+9T>A	ENSP00000512126.1:n.413+9T>A
ENST00000695734.1:c.413+9T>A	ENSP00000512127.1:n.413+9T>A
ENST00000695736.1:c.77+9T>A	ENSP00000512129.1:n.77+9T>A
XM_005256115.2:c.671+9T>A	XP_005256172.1:n.671+9T>A
XM_005256115.4:c.671+9T>A	XP_005256172.1:n.671+9T>A
XR_429727.2:n.1008+9T>A
XR_429727.3:n.1021+9T>A
XR_429728.2:n.1008+9T>A
XR_429728.3:n.1025+9T>A