Canonical Allele Identifier: CA496087527

Gene: ACD

Linked Data

• MyVariant Identifiers: chr16:g.67691691G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67657788G>C , CM000678.2:g.67657788G>C	GRCh38
NC_000016.9:g.67691691G>C , CM000678.1:g.67691691G>C	GRCh37
NC_000016.8:g.66249192G>C	NCBI36
NG_042874.1:g.8028C>G
NG_054728.1:g.17870G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000602382.6:c.938C>G	ENSP00000473313.2:p.Pro313Arg
ENST00000602780.2:n.2277C>G
ENST00000602860.6:n.2192C>G
ENST00000695641.1:n.2381C>G
ENST00000695648.1:c.1254C>G	ENSP00000512081.1:p.Ser418=
ENST00000695656.1:n.2232C>G
ENST00000695657.1:n.1590C>G
ENST00000695658.1:c.1095C>G	ENSP00000512088.1:p.Ser365=
ENST00000695659.1:c.1290C>G	ENSP00000512089.1:p.Ser430=
ENST00000695662.1:c.*751C>G	ENSP00000512091.1:n.*751C>G
ENST00000695694.1:c.1227C>G	ENSP00000512105.1:p.Ser409=
ENST00000695695.1:n.1338C>G
ENST00000695696.1:n.1319C>G
ENST00000695697.1:c.1185C>G	ENSP00000512106.1:p.Ser395=
ENST00000695698.1:n.1522C>G
ENST00000695699.1:n.1692C>G
ENST00000695709.1:n.547C>G
ENST00000695710.1:n.1906C>G
ENST00000695711.1:c.*580C>G	ENSP00000512109.1:n.*580C>G
ENST00000695712.1:c.*1022C>G	ENSP00000512110.1:n.*1022C>G
ENST00000695731.1:c.595C>G
ENST00000695732.1:c.711C>G	ENSP00000512125.1:p.Ser237=
ENST00000695733.1:c.851C>G	ENSP00000512126.1:p.Pro284Arg
ENST00000695734.1:c.1272C>G	ENSP00000512127.1:p.Ser424=
ENST00000219251.13:c.1263C>G	ENSP00000219251.8:p.Ser421=
ENST00000620761.6:c.1272C>G MANE Select	ENSP00000478084.1:p.Ser424=
ENST00000219251.12:c.1521C>G	ENSP00000219251.7:p.Ser507=
ENST00000393919.8:c.1530C>G	ENSP00000377496.4:p.Ser510=
ENST00000602320.1:c.1224C>G	ENSP00000473679.2:p.Ser408=
ENST00000602382.5:c.480C>G
ENST00000602622.5:n.2271C>G
ENST00000602656.1:n.536C>G
ENST00000602860.5:n.1710C>G
ENST00000620338.4:c.1530C>G	ENSP00000483117.1:p.Ser510=
ENST00000620761.4:c.1272C>G	ENSP00000478084.1:p.Ser424=
NM_001082486.1:c.1530C>G	NP_001075955.1:p.Ser510=
NM_001082487.1:c.1482C>G	NP_001075956.1:p.Ser494=
NM_022914.2:c.1521C>G	NP_075065.2:p.Ser507=
XM_005256115.2:c.1443C>G	XP_005256172.1:p.Ser481=
NM_001082486.2:c.1272C>G MANE Select	NP_001075955.2:p.Ser424=
NM_022914.3:c.1263C>G	NP_075065.3:p.Ser421=
XM_005256115.4:c.1443C>G	XP_005256172.1:p.Ser481=