Canonical Allele Identifier: CA623120798

Gene: ACD

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67657745C>T , CM000678.2:g.67657745C>T	GRCh38
NC_000016.9:g.67691648C>T , CM000678.1:g.67691648C>T	GRCh37
NC_000016.8:g.66249149C>T	NCBI36
NG_042874.1:g.8071G>A
NG_054728.1:g.17827C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000602382.6:c.964+17G>A	ENSP00000473313.2:n.964+17G>A
ENST00000602780.2:n.2320G>A
ENST00000602860.6:n.2218+17G>A
ENST00000695641.1:n.2407+17G>A
ENST00000695648.1:c.1280+17G>A	ENSP00000512081.1:n.1280+17G>A
ENST00000695656.1:n.2275G>A
ENST00000695657.1:n.1616+17G>A
ENST00000695658.1:c.1121+17G>A	ENSP00000512088.1:n.1121+17G>A
ENST00000695659.1:c.1316+17G>A	ENSP00000512089.1:n.1316+17G>A
ENST00000695662.1:c.*777+17G>A	ENSP00000512091.1:n.*777+17G>A
ENST00000695694.1:c.1253+17G>A	ENSP00000512105.1:n.1253+17G>A
ENST00000695695.1:n.1364+17G>A
ENST00000695696.1:n.1345+17G>A
ENST00000695697.1:c.1211+17G>A	ENSP00000512106.1:n.1211+17G>A
ENST00000695698.1:n.1548+17G>A
ENST00000695709.1:n.573+17G>A
ENST00000695711.1:c.*606+17G>A	ENSP00000512109.1:n.*606+17G>A
ENST00000695712.1:c.*1048+17G>A	ENSP00000512110.1:n.*1048+17G>A
ENST00000695731.1:c.621+17G>A
ENST00000695732.1:c.737+17G>A	ENSP00000512125.1:n.737+17G>A
ENST00000695733.1:c.877+17G>A	ENSP00000512126.1:n.877+17G>A
ENST00000695734.1:c.1298+17G>A	ENSP00000512127.1:n.1298+17G>A
ENST00000219251.13:c.1289+17G>A	ENSP00000219251.8:n.1289+17G>A
ENST00000620761.6:c.1298+17G>A MANE Select	ENSP00000478084.1:n.1298+17G>A
ENST00000219251.12:c.1547+17G>A	ENSP00000219251.7:n.1547+17G>A
ENST00000393919.8:c.1556+17G>A	ENSP00000377496.4:n.1556+17G>A
ENST00000602320.1:c.1250+17G>A	ENSP00000473679.2:n.1250+17G>A
ENST00000602382.5:c.506+17G>A
ENST00000602622.5:n.2314G>A
ENST00000602656.1:n.562+17G>A
ENST00000602860.5:n.1736+17G>A
ENST00000620338.4:c.1556+17G>A	ENSP00000483117.1:n.1556+17G>A
ENST00000620761.4:c.1298+17G>A	ENSP00000478084.1:n.1298+17G>A
NM_001082486.1:c.1556+17G>A	NP_001075955.1:n.1556+17G>A
NM_001082487.1:c.1508+17G>A	NP_001075956.1:n.1508+17G>A
NM_022914.2:c.1547+17G>A	NP_075065.2:n.1547+17G>A
XM_005256115.2:c.1469+17G>A	XP_005256172.1:n.1469+17G>A
NM_001082486.2:c.1298+17G>A MANE Select	NP_001075955.2:n.1298+17G>A
NM_022914.3:c.1289+17G>A	NP_075065.3:n.1289+17G>A
XM_005256115.4:c.1469+17G>A	XP_005256172.1:n.1469+17G>A