Canonical Allele Identifier: CA270736

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 156285
• ClinVar RCV Id: RCV000144369 ; RCV003480060
• dbSNP Id: rs137853282
• MyVariant Identifiers: chr13:g.52532465C>T (hg19) ; chr13:g.51958329C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*170G>A	ENSP00000489512.2:n.*170G>A
ENST00000673864.2:c.*1081G>A	ENSP00000501045.2:n.*1081G>A
ENST00000674147.2:c.1870-722G>A	ENSP00000500964.2:n.1870-722G>A
ENST00000242839.10:c.2337G>A MANE Select	ENSP00000242839.5:p.Trp779Ter
ENST00000344297.9:c.1870-722G>A	ENSP00000342559.5:n.1870-722G>A
ENST00000400366.6:c.2004G>A	ENSP00000383217.3:p.Trp668Ter
ENST00000448424.7:c.2085G>A	ENSP00000416738.3:p.Trp695Ter
ENST00000673772.1:c.2122-722G>A	ENSP00000501168.1:n.2122-722G>A
ENST00000674147.1:c.1426-722G>A	ENSP00000500964.1:n.1426-722G>A
ENST00000242839.8:c.2337G>A	ENSP00000242839.4:p.Trp779Ter
ENST00000344297.8:c.1870-722G>A	ENSP00000342559.5:n.1870-722G>A
ENST00000400366.5:c.2004G>A	ENSP00000383217.3:p.Trp668Ter
ENST00000400370.8:c.1286-8168G>A	ENSP00000383221.3:n.1286-8168G>A
ENST00000418097.7:c.2337G>A	ENSP00000393343.2:p.Trp779Ter
ENST00000448424.6:c.2122-722G>A	ENSP00000416738.2:n.2122-722G>A
ENST00000634296.1:c.298G>A
ENST00000634308.1:c.2122-722G>A	ENSP00000489234.1:n.2122-722G>A
ENST00000634620.1:n.2432G>A
ENST00000634810.1:n.1682G>A
ENST00000634844.1:c.2193G>A	ENSP00000489398.1:p.Trp731Ter
ENST00000635406.1:n.212-11851G>A
NM_000053.3:c.2337G>A	NP_000044.2:p.Trp779Ter
NM_001005918.2:c.1870-722G>A	NP_001005918.1:n.1870-722G>A
NM_001243182.1:c.2004G>A	NP_001230111.1:p.Trp668Ter
XM_005266423.2:c.2241G>A	XP_005266480.1:p.Trp747Ter
XM_005266424.3:c.2241G>A	XP_005266481.1:p.Trp747Ter
XM_005266427.2:c.2122-722G>A	XP_005266484.1:n.2122-722G>A
XM_005266428.1:c.2085G>A	XP_005266485.1:p.Trp695Ter
XM_005266430.3:c.2337G>A	XP_005266487.1:p.Trp779Ter
XM_005266431.2:c.2301G>A	XP_005266488.1:p.Trp767Ter
XM_005266432.2:c.1870-722G>A	XP_005266489.1:n.1870-722G>A
XM_006719837.2:c.2241G>A	XP_006719900.1:p.Trp747Ter
XM_006719838.1:c.153G>A	XP_006719901.1:p.Trp51Ter
XM_006719839.1:c.153G>A	XP_006719902.1:p.Trp51Ter
XM_011535117.1:c.2241G>A	XP_011533419.1:p.Trp747Ter
XM_011535118.1:c.2337G>A	XP_011533420.1:p.Trp779Ter
XM_011535119.1:c.2337G>A	XP_011533421.1:p.Trp779Ter
XM_011535120.1:c.1923G>A	XP_011533422.1:p.Trp641Ter
XM_011535121.1:c.2337G>A	XP_011533423.1:p.Trp779Ter
XM_011535122.1:c.1005G>A	XP_011533424.1:p.Trp335Ter
XR_941601.1:n.2556G>A
XR_941602.1:n.2556G>A
XR_941603.1:n.2556G>A
XR_941604.1:n.2556G>A
NM_001330578.1:c.2122-722G>A	NP_001317507.1:n.2122-722G>A
NM_001330579.1:c.2085G>A	NP_001317508.1:p.Trp695Ter
XM_005266424.4:c.2241G>A	XP_005266481.1:p.Trp747Ter
XM_005266430.4:c.2337G>A	XP_005266487.1:p.Trp779Ter
XM_005266431.4:c.2301G>A	XP_005266488.1:p.Trp767Ter
XM_006719837.3:c.2241G>A	XP_006719900.1:p.Trp747Ter
XM_011535117.3:c.2241G>A	XP_011533419.1:p.Trp747Ter
XM_017020627.1:c.2241G>A	XP_016876116.1:p.Trp747Ter
NM_000053.4:c.2337G>A MANE Select	NP_000044.2:p.Trp779Ter
NM_001005918.3:c.1870-722G>A	NP_001005918.1:n.1870-722G>A
NM_001330579.2:c.2085G>A	NP_001317508.1:p.Trp695Ter
NM_001243182.2:c.2004G>A	NP_001230111.1:p.Trp668Ter
NM_001330578.2:c.2122-722G>A	NP_001317507.1:n.2122-722G>A