Canonical Allele Identifier: CA388020480

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 1172922
• ClinVar RCV Id: RCV001527078
• dbSNP Id: rs137853282
• MyVariant Identifiers: chr13:g.52532465C>G (hg19) ; chr13:g.51958329C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51958329C>G , CM000675.2:g.51958329C>G	GRCh38
NC_000013.10:g.52532465C>G , CM000675.1:g.52532465C>G	GRCh37
NC_000013.9:g.51430466C>G	NCBI36
NG_008806.1:g.58166G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*170G>C	ENSP00000489512.2:n.*170G>C
ENST00000673864.2:c.*1081G>C	ENSP00000501045.2:n.*1081G>C
ENST00000674147.2:c.1870-722G>C	ENSP00000500964.2:n.1870-722G>C
ENST00000242839.10:c.2337G>C MANE Select	ENSP00000242839.5:p.Trp779Cys
ENST00000344297.9:c.1870-722G>C	ENSP00000342559.5:n.1870-722G>C
ENST00000400366.6:c.2004G>C	ENSP00000383217.3:p.Trp668Cys
ENST00000448424.7:c.2085G>C	ENSP00000416738.3:p.Trp695Cys
ENST00000673772.1:c.2122-722G>C	ENSP00000501168.1:n.2122-722G>C
ENST00000674147.1:c.1426-722G>C	ENSP00000500964.1:n.1426-722G>C
ENST00000242839.8:c.2337G>C	ENSP00000242839.4:p.Trp779Cys
ENST00000344297.8:c.1870-722G>C	ENSP00000342559.5:n.1870-722G>C
ENST00000400366.5:c.2004G>C	ENSP00000383217.3:p.Trp668Cys
ENST00000400370.8:c.1286-8168G>C	ENSP00000383221.3:n.1286-8168G>C
ENST00000418097.7:c.2337G>C	ENSP00000393343.2:p.Trp779Cys
ENST00000448424.6:c.2122-722G>C	ENSP00000416738.2:n.2122-722G>C
ENST00000634296.1:c.298G>C
ENST00000634308.1:c.2122-722G>C	ENSP00000489234.1:n.2122-722G>C
ENST00000634620.1:n.2432G>C
ENST00000634810.1:n.1682G>C
ENST00000634844.1:c.2193G>C	ENSP00000489398.1:p.Trp731Cys
ENST00000635406.1:n.212-11851G>C
NM_000053.3:c.2337G>C	NP_000044.2:p.Trp779Cys
NM_001005918.2:c.1870-722G>C	NP_001005918.1:n.1870-722G>C
NM_001243182.1:c.2004G>C	NP_001230111.1:p.Trp668Cys
XM_005266423.2:c.2241G>C	XP_005266480.1:p.Trp747Cys
XM_005266424.3:c.2241G>C	XP_005266481.1:p.Trp747Cys
XM_005266427.2:c.2122-722G>C	XP_005266484.1:n.2122-722G>C
XM_005266428.1:c.2085G>C	XP_005266485.1:p.Trp695Cys
XM_005266430.3:c.2337G>C	XP_005266487.1:p.Trp779Cys
XM_005266431.2:c.2301G>C	XP_005266488.1:p.Trp767Cys
XM_005266432.2:c.1870-722G>C	XP_005266489.1:n.1870-722G>C
XM_006719837.2:c.2241G>C	XP_006719900.1:p.Trp747Cys
XM_006719838.1:c.153G>C	XP_006719901.1:p.Trp51Cys
XM_006719839.1:c.153G>C	XP_006719902.1:p.Trp51Cys
XM_011535117.1:c.2241G>C	XP_011533419.1:p.Trp747Cys
XM_011535118.1:c.2337G>C	XP_011533420.1:p.Trp779Cys
XM_011535119.1:c.2337G>C	XP_011533421.1:p.Trp779Cys
XM_011535120.1:c.1923G>C	XP_011533422.1:p.Trp641Cys
XM_011535121.1:c.2337G>C	XP_011533423.1:p.Trp779Cys
XM_011535122.1:c.1005G>C	XP_011533424.1:p.Trp335Cys
XR_941601.1:n.2556G>C
XR_941602.1:n.2556G>C
XR_941603.1:n.2556G>C
XR_941604.1:n.2556G>C
NM_001330578.1:c.2122-722G>C	NP_001317507.1:n.2122-722G>C
NM_001330579.1:c.2085G>C	NP_001317508.1:p.Trp695Cys
XM_005266424.4:c.2241G>C	XP_005266481.1:p.Trp747Cys
XM_005266430.4:c.2337G>C	XP_005266487.1:p.Trp779Cys
XM_005266431.4:c.2301G>C	XP_005266488.1:p.Trp767Cys
XM_006719837.3:c.2241G>C	XP_006719900.1:p.Trp747Cys
XM_011535117.3:c.2241G>C	XP_011533419.1:p.Trp747Cys
XM_017020627.1:c.2241G>C	XP_016876116.1:p.Trp747Cys
NM_000053.4:c.2337G>C MANE Select	NP_000044.2:p.Trp779Cys
NM_001005918.3:c.1870-722G>C	NP_001005918.1:n.1870-722G>C
NM_001330579.2:c.2085G>C	NP_001317508.1:p.Trp695Cys
NM_001243182.2:c.2004G>C	NP_001230111.1:p.Trp668Cys
NM_001330578.2:c.2122-722G>C	NP_001317507.1:n.2122-722G>C