Canonical Allele Identifier: CA496087587

Gene: ACD

Linked Data

• MyVariant Identifiers: chr16:g.67691730A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67657827A>C , CM000678.2:g.67657827A>C	GRCh38
NC_000016.9:g.67691730A>C , CM000678.1:g.67691730A>C	GRCh37
NC_000016.8:g.66249231A>C	NCBI36
NG_042874.1:g.7989T>G
NG_054728.1:g.17909A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000602382.6:c.899T>G	ENSP00000473313.2:p.Val300Gly
ENST00000602780.2:n.2238T>G
ENST00000602860.6:n.2153T>G
ENST00000695641.1:n.2342T>G
ENST00000695648.1:c.1215T>G	ENSP00000512081.1:p.Gly405=
ENST00000695656.1:n.2193T>G
ENST00000695657.1:n.1551T>G
ENST00000695658.1:c.1056T>G	ENSP00000512088.1:p.Gly352=
ENST00000695659.1:c.1251T>G	ENSP00000512089.1:p.Gly417=
ENST00000695662.1:c.*712T>G	ENSP00000512091.1:n.*712T>G
ENST00000695694.1:c.1188T>G	ENSP00000512105.1:p.Gly396=
ENST00000695695.1:n.1299T>G
ENST00000695696.1:n.1280T>G
ENST00000695697.1:c.1146T>G	ENSP00000512106.1:p.Gly382=
ENST00000695698.1:n.1483T>G
ENST00000695699.1:n.1653T>G
ENST00000695709.1:n.508T>G
ENST00000695710.1:n.1867T>G
ENST00000695711.1:c.*541T>G	ENSP00000512109.1:n.*541T>G
ENST00000695712.1:c.*983T>G	ENSP00000512110.1:n.*983T>G
ENST00000695731.1:c.556T>G
ENST00000695732.1:c.672T>G	ENSP00000512125.1:p.Gly224=
ENST00000695733.1:c.812T>G	ENSP00000512126.1:p.Val271Gly
ENST00000695734.1:c.1233T>G	ENSP00000512127.1:p.Gly411=
ENST00000219251.13:c.1224T>G	ENSP00000219251.8:p.Gly408=
ENST00000620761.6:c.1233T>G MANE Select	ENSP00000478084.1:p.Gly411=
ENST00000219251.12:c.1482T>G	ENSP00000219251.7:p.Gly494=
ENST00000393919.8:c.1491T>G	ENSP00000377496.4:p.Gly497=
ENST00000602320.1:c.1198-13T>G	ENSP00000473679.2:n.1198-13T>G
ENST00000602382.5:c.441T>G
ENST00000602622.5:n.2232T>G
ENST00000602656.1:n.497T>G
ENST00000602860.5:n.1671T>G
ENST00000620338.4:c.1491T>G	ENSP00000483117.1:p.Gly497=
ENST00000620761.4:c.1233T>G	ENSP00000478084.1:p.Gly411=
NM_001082486.1:c.1491T>G	NP_001075955.1:p.Gly497=
NM_001082487.1:c.1456-13T>G	NP_001075956.1:n.1456-13T>G
NM_022914.2:c.1482T>G	NP_075065.2:p.Gly494=
XM_005256115.2:c.1404T>G	XP_005256172.1:p.Gly468=
NM_001082486.2:c.1233T>G MANE Select	NP_001075955.2:p.Gly411=
NM_022914.3:c.1224T>G	NP_075065.3:p.Gly408=
XM_005256115.4:c.1404T>G	XP_005256172.1:p.Gly468=