Canonical Allele Identifier: CA2229422953

Gene: ACD

Linked Data

• dbSNP Id: rs2052897519

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67657712del , CM000678.2:g.67657712del	GRCh38
NC_000016.9:g.67691615del , CM000678.1:g.67691615del	GRCh37
NC_000016.8:g.66249116del	NCBI36
NG_042874.1:g.8105del
NG_054728.1:g.17794del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000602382.6:c.965-27del	ENSP00000473313.2:n.965-27del
ENST00000602780.2:n.2354del
ENST00000602860.6:n.2219-27del
ENST00000695641.1:n.2408-27del
ENST00000695648.1:c.1281-27del	ENSP00000512081.1:n.1281-27del
ENST00000695656.1:n.2309del
ENST00000695657.1:n.1617-27del
ENST00000695658.1:c.1122-27del	ENSP00000512088.1:n.1122-27del
ENST00000695659.1:c.1317-27del	ENSP00000512089.1:n.1317-27del
ENST00000695662.1:c.*778-27del	ENSP00000512091.1:n.*778-27del
ENST00000695694.1:c.1254-27del	ENSP00000512105.1:n.1254-27del
ENST00000695695.1:n.1365-27del
ENST00000695696.1:n.1346-27del
ENST00000695697.1:c.1212-27del	ENSP00000512106.1:n.1212-27del
ENST00000695698.1:n.1549-27del
ENST00000695709.1:n.574-27del
ENST00000695711.1:c.*607-27del	ENSP00000512109.1:n.*607-27del
ENST00000695712.1:c.*1049-27del	ENSP00000512110.1:n.*1049-27del
ENST00000695731.1:c.622-27del
ENST00000695732.1:c.738-27del	ENSP00000512125.1:n.738-27del
ENST00000695733.1:c.878-27del	ENSP00000512126.1:n.878-27del
ENST00000695734.1:c.1299-10del	ENSP00000512127.1:n.1299-10del
ENST00000219251.13:c.1290-27del	ENSP00000219251.8:n.1290-27del
ENST00000620761.6:c.1299-27del MANE Select	ENSP00000478084.1:n.1299-27del
ENST00000219251.12:c.1548-27del	ENSP00000219251.7:n.1548-27del
ENST00000393919.8:c.1557-27del	ENSP00000377496.4:n.1557-27del
ENST00000602320.1:c.1251-27del	ENSP00000473679.2:n.1251-27del
ENST00000602382.5:c.507-27del
ENST00000602622.5:n.2348del
ENST00000602656.1:n.563-27del
ENST00000602860.5:n.1737-27del
ENST00000620338.4:c.1557-27del	ENSP00000483117.1:n.1557-27del
ENST00000620761.4:c.1299-27del	ENSP00000478084.1:n.1299-27del
NM_001082486.1:c.1557-27del	NP_001075955.1:n.1557-27del
NM_001082487.1:c.1509-27del	NP_001075956.1:n.1509-27del
NM_022914.2:c.1548-27del	NP_075065.2:n.1548-27del
XM_005256115.2:c.1470-27del	XP_005256172.1:n.1470-27del
NM_001082486.2:c.1299-27del MANE Select	NP_001075955.2:n.1299-27del
NM_022914.3:c.1290-27del	NP_075065.3:n.1290-27del
XM_005256115.4:c.1470-27del	XP_005256172.1:n.1470-27del