Canonical Allele Identifier: CA396349755

Gene: ACD

Linked Data

• MyVariant Identifiers: chr16:g.67691589T>G (hg19) ; chr16:g.67657686T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67657686T>G , CM000678.2:g.67657686T>G	GRCh38
NC_000016.9:g.67691589T>G , CM000678.1:g.67691589T>G	GRCh37
NC_000016.8:g.66249090T>G	NCBI36
NG_042874.1:g.8130A>C
NG_054728.1:g.17768T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000602382.6:c.965-2A>C	ENSP00000473313.2:n.965-2A>C
ENST00000602780.2:n.2379A>C
ENST00000602860.6:n.2219-2A>C
ENST00000695641.1:n.2408-2A>C
ENST00000695648.1:c.1281-2A>C	ENSP00000512081.1:n.1281-2A>C
ENST00000695656.1:n.2334A>C
ENST00000695657.1:n.1617-2A>C
ENST00000695658.1:c.1122-2A>C	ENSP00000512088.1:n.1122-2A>C
ENST00000695659.1:c.1317-2A>C	ENSP00000512089.1:n.1317-2A>C
ENST00000695662.1:c.*778-2A>C	ENSP00000512091.1:n.*778-2A>C
ENST00000695694.1:c.1254-2A>C	ENSP00000512105.1:n.1254-2A>C
ENST00000695695.1:n.1365-2A>C
ENST00000695696.1:n.1346-2A>C
ENST00000695697.1:c.1212-2A>C	ENSP00000512106.1:n.1212-2A>C
ENST00000695698.1:n.1549-2A>C
ENST00000695709.1:n.574-2A>C
ENST00000695711.1:c.*607-2A>C	ENSP00000512109.1:n.*607-2A>C
ENST00000695712.1:c.*1049-2A>C	ENSP00000512110.1:n.*1049-2A>C
ENST00000695731.1:c.622-2A>C
ENST00000695732.1:c.738-2A>C	ENSP00000512125.1:n.738-2A>C
ENST00000695733.1:c.878-2A>C	ENSP00000512126.1:n.878-2A>C
ENST00000695734.1:c.1314A>C	ENSP00000512127.1:p.Pro438=
ENST00000219251.13:c.1290-2A>C	ENSP00000219251.8:n.1290-2A>C
ENST00000620761.6:c.1299-2A>C MANE Select	ENSP00000478084.1:n.1299-2A>C
ENST00000219251.12:c.1548-2A>C	ENSP00000219251.7:n.1548-2A>C
ENST00000393919.8:c.1557-2A>C	ENSP00000377496.4:n.1557-2A>C
ENST00000602320.1:c.1251-2A>C	ENSP00000473679.2:n.1251-2A>C
ENST00000602382.5:c.507-2A>C
ENST00000602622.5:n.2373A>C
ENST00000602656.1:n.563-2A>C
ENST00000602860.5:n.1737-2A>C
ENST00000620338.4:c.1557-2A>C	ENSP00000483117.1:n.1557-2A>C
ENST00000620761.4:c.1299-2A>C	ENSP00000478084.1:n.1299-2A>C
NM_001082486.1:c.1557-2A>C	NP_001075955.1:n.1557-2A>C
NM_001082487.1:c.1509-2A>C	NP_001075956.1:n.1509-2A>C
NM_022914.2:c.1548-2A>C	NP_075065.2:n.1548-2A>C
XM_005256115.2:c.1470-2A>C	XP_005256172.1:n.1470-2A>C
NM_001082486.2:c.1299-2A>C MANE Select	NP_001075955.2:n.1299-2A>C
NM_022914.3:c.1290-2A>C	NP_075065.3:n.1290-2A>C
XM_005256115.4:c.1470-2A>C	XP_005256172.1:n.1470-2A>C