Canonical Allele Identifier: CA496087604

Gene: ACD

Linked Data

• MyVariant Identifiers: chr16:g.67691744T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67657841T>G , CM000678.2:g.67657841T>G	GRCh38
NC_000016.9:g.67691744T>G , CM000678.1:g.67691744T>G	GRCh37
NC_000016.8:g.66249245T>G	NCBI36
NG_042874.1:g.7975A>C
NG_054728.1:g.17923T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000602382.6:c.885A>C	ENSP00000473313.2:p.Arg295Ser
ENST00000602780.2:n.2224A>C
ENST00000602860.6:n.2139A>C
ENST00000695641.1:n.2328A>C
ENST00000695648.1:c.1201A>C	ENSP00000512081.1:p.Arg401=
ENST00000695656.1:n.2179A>C
ENST00000695657.1:n.1537A>C
ENST00000695658.1:c.1042A>C	ENSP00000512088.1:p.Arg348=
ENST00000695659.1:c.1237A>C	ENSP00000512089.1:p.Arg413=
ENST00000695662.1:c.*698A>C	ENSP00000512091.1:n.*698A>C
ENST00000695694.1:c.1174A>C	ENSP00000512105.1:p.Arg392=
ENST00000695695.1:n.1285A>C
ENST00000695696.1:n.1266A>C
ENST00000695697.1:c.1132A>C	ENSP00000512106.1:p.Arg378=
ENST00000695698.1:n.1469A>C
ENST00000695699.1:n.1639A>C
ENST00000695709.1:n.494A>C
ENST00000695710.1:n.1853A>C
ENST00000695711.1:c.*527A>C	ENSP00000512109.1:n.*527A>C
ENST00000695712.1:c.*969A>C	ENSP00000512110.1:n.*969A>C
ENST00000695731.1:c.542A>C
ENST00000695732.1:c.658A>C	ENSP00000512125.1:p.Arg220=
ENST00000695733.1:c.798A>C	ENSP00000512126.1:p.Arg266Ser
ENST00000695734.1:c.1219A>C	ENSP00000512127.1:p.Arg407=
ENST00000219251.13:c.1210A>C	ENSP00000219251.8:p.Arg404=
ENST00000620761.6:c.1219A>C MANE Select	ENSP00000478084.1:p.Arg407=
ENST00000219251.12:c.1468A>C	ENSP00000219251.7:p.Arg490=
ENST00000393919.8:c.1477A>C	ENSP00000377496.4:p.Arg493=
ENST00000602320.1:c.1198-27A>C	ENSP00000473679.2:n.1198-27A>C
ENST00000602382.5:c.427A>C
ENST00000602622.5:n.2218A>C
ENST00000602656.1:n.483A>C
ENST00000602860.5:n.1657A>C
ENST00000620338.4:c.1477A>C	ENSP00000483117.1:p.Arg493=
ENST00000620761.4:c.1219A>C	ENSP00000478084.1:p.Arg407=
NM_001082486.1:c.1477A>C	NP_001075955.1:p.Arg493=
NM_001082487.1:c.1456-27A>C	NP_001075956.1:n.1456-27A>C
NM_022914.2:c.1468A>C	NP_075065.2:p.Arg490=
XM_005256115.2:c.1390A>C	XP_005256172.1:p.Arg464=
NM_001082486.2:c.1219A>C MANE Select	NP_001075955.2:p.Arg407=
NM_022914.3:c.1210A>C	NP_075065.3:p.Arg404=
XM_005256115.4:c.1390A>C	XP_005256172.1:p.Arg464=