Canonical Allele Identifier: CA623120766

Gene: ACD

Linked Data

• dbSNP Id: rs1313644620
• gnomAD v2: 16-67691599-C-T
• MyVariant Identifiers: chr16:g.67691599C>T (hg19) ; chr16:g.67657696C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67657696C>T , CM000678.2:g.67657696C>T	GRCh38
NC_000016.9:g.67691599C>T , CM000678.1:g.67691599C>T	GRCh37
NC_000016.8:g.66249100C>T	NCBI36
NG_042874.1:g.8120G>A
NG_054728.1:g.17778C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000602382.6:c.965-12G>A	ENSP00000473313.2:n.965-12G>A
ENST00000602780.2:n.2369G>A
ENST00000602860.6:n.2219-12G>A
ENST00000695641.1:n.2408-12G>A
ENST00000695648.1:c.1281-12G>A	ENSP00000512081.1:n.1281-12G>A
ENST00000695656.1:n.2324G>A
ENST00000695657.1:n.1617-12G>A
ENST00000695658.1:c.1122-12G>A	ENSP00000512088.1:n.1122-12G>A
ENST00000695659.1:c.1317-12G>A	ENSP00000512089.1:n.1317-12G>A
ENST00000695662.1:c.*778-12G>A	ENSP00000512091.1:n.*778-12G>A
ENST00000695694.1:c.1254-12G>A	ENSP00000512105.1:n.1254-12G>A
ENST00000695695.1:n.1365-12G>A
ENST00000695696.1:n.1346-12G>A
ENST00000695697.1:c.1212-12G>A	ENSP00000512106.1:n.1212-12G>A
ENST00000695698.1:n.1549-12G>A
ENST00000695709.1:n.574-12G>A
ENST00000695711.1:c.*607-12G>A	ENSP00000512109.1:n.*607-12G>A
ENST00000695712.1:c.*1049-12G>A	ENSP00000512110.1:n.*1049-12G>A
ENST00000695731.1:c.622-12G>A
ENST00000695732.1:c.738-12G>A	ENSP00000512125.1:n.738-12G>A
ENST00000695733.1:c.878-12G>A	ENSP00000512126.1:n.878-12G>A
ENST00000695734.1:c.1304G>A	ENSP00000512127.1:p.Gly435Asp
ENST00000219251.13:c.1290-12G>A	ENSP00000219251.8:n.1290-12G>A
ENST00000620761.6:c.1299-12G>A MANE Select	ENSP00000478084.1:n.1299-12G>A
ENST00000219251.12:c.1548-12G>A	ENSP00000219251.7:n.1548-12G>A
ENST00000393919.8:c.1557-12G>A	ENSP00000377496.4:n.1557-12G>A
ENST00000602320.1:c.1251-12G>A	ENSP00000473679.2:n.1251-12G>A
ENST00000602382.5:c.507-12G>A
ENST00000602622.5:n.2363G>A
ENST00000602656.1:n.563-12G>A
ENST00000602860.5:n.1737-12G>A
ENST00000620338.4:c.1557-12G>A	ENSP00000483117.1:n.1557-12G>A
ENST00000620761.4:c.1299-12G>A	ENSP00000478084.1:n.1299-12G>A
NM_001082486.1:c.1557-12G>A	NP_001075955.1:n.1557-12G>A
NM_001082487.1:c.1509-12G>A	NP_001075956.1:n.1509-12G>A
NM_022914.2:c.1548-12G>A	NP_075065.2:n.1548-12G>A
XM_005256115.2:c.1470-12G>A	XP_005256172.1:n.1470-12G>A
NM_001082486.2:c.1299-12G>A MANE Select	NP_001075955.2:n.1299-12G>A
NM_022914.3:c.1290-12G>A	NP_075065.3:n.1290-12G>A
XM_005256115.4:c.1470-12G>A	XP_005256172.1:n.1470-12G>A