Canonical Allele Identifier: CA496087584

Gene: ACD

Linked Data

• MyVariant Identifiers: chr16:g.67691727A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67657824A>T , CM000678.2:g.67657824A>T	GRCh38
NC_000016.9:g.67691727A>T , CM000678.1:g.67691727A>T	GRCh37
NC_000016.8:g.66249228A>T	NCBI36
NG_042874.1:g.7992T>A
NG_054728.1:g.17906A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000602382.6:c.902T>A	ENSP00000473313.2:p.Leu301Gln
ENST00000602780.2:n.2241T>A
ENST00000602860.6:n.2156T>A
ENST00000695641.1:n.2345T>A
ENST00000695648.1:c.1218T>A	ENSP00000512081.1:p.Ser406=
ENST00000695656.1:n.2196T>A
ENST00000695657.1:n.1554T>A
ENST00000695658.1:c.1059T>A	ENSP00000512088.1:p.Ser353=
ENST00000695659.1:c.1254T>A	ENSP00000512089.1:p.Ser418=
ENST00000695662.1:c.*715T>A	ENSP00000512091.1:n.*715T>A
ENST00000695694.1:c.1191T>A	ENSP00000512105.1:p.Ser397=
ENST00000695695.1:n.1302T>A
ENST00000695696.1:n.1283T>A
ENST00000695697.1:c.1149T>A	ENSP00000512106.1:p.Ser383=
ENST00000695698.1:n.1486T>A
ENST00000695699.1:n.1656T>A
ENST00000695709.1:n.511T>A
ENST00000695710.1:n.1870T>A
ENST00000695711.1:c.*544T>A	ENSP00000512109.1:n.*544T>A
ENST00000695712.1:c.*986T>A	ENSP00000512110.1:n.*986T>A
ENST00000695731.1:c.559T>A
ENST00000695732.1:c.675T>A	ENSP00000512125.1:p.Ser225=
ENST00000695733.1:c.815T>A	ENSP00000512126.1:p.Leu272Gln
ENST00000695734.1:c.1236T>A	ENSP00000512127.1:p.Ser412=
ENST00000219251.13:c.1227T>A	ENSP00000219251.8:p.Ser409=
ENST00000620761.6:c.1236T>A MANE Select	ENSP00000478084.1:p.Ser412=
ENST00000219251.12:c.1485T>A	ENSP00000219251.7:p.Ser495=
ENST00000393919.8:c.1494T>A	ENSP00000377496.4:p.Ser498=
ENST00000602320.1:c.1198-10T>A	ENSP00000473679.2:n.1198-10T>A
ENST00000602382.5:c.444T>A
ENST00000602622.5:n.2235T>A
ENST00000602656.1:n.500T>A
ENST00000602860.5:n.1674T>A
ENST00000620338.4:c.1494T>A	ENSP00000483117.1:p.Ser498=
ENST00000620761.4:c.1236T>A	ENSP00000478084.1:p.Ser412=
NM_001082486.1:c.1494T>A	NP_001075955.1:p.Ser498=
NM_001082487.1:c.1456-10T>A	NP_001075956.1:n.1456-10T>A
NM_022914.2:c.1485T>A	NP_075065.2:p.Ser495=
XM_005256115.2:c.1407T>A	XP_005256172.1:p.Ser469=
NM_001082486.2:c.1236T>A MANE Select	NP_001075955.2:p.Ser412=
NM_022914.3:c.1227T>A	NP_075065.3:p.Ser409=
XM_005256115.4:c.1407T>A	XP_005256172.1:p.Ser469=