Canonical Allele Identifier: CA388032469

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52520579G>C (hg19) ; chr13:g.51946443G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946443G>C , CM000675.2:g.51946443G>C	GRCh38
NC_000013.10:g.52520579G>C , CM000675.1:g.52520579G>C	GRCh37
NC_000013.9:g.51418580G>C	NCBI36
NG_008806.1:g.70052C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*734C>G	ENSP00000489512.2:n.*734C>G
ENST00000673864.2:c.*1645C>G	ENSP00000501045.2:n.*1645C>G
ENST00000674147.2:c.2280C>G	ENSP00000500964.2:p.Ile760Met
ENST00000242839.10:c.2901C>G MANE Select	ENSP00000242839.5:p.Ile967Met
ENST00000344297.9:c.2280C>G	ENSP00000342559.5:p.Ile760Met
ENST00000400366.6:c.2568C>G	ENSP00000383217.3:p.Ile856Met
ENST00000448424.7:c.2649C>G	ENSP00000416738.3:p.Ile883Met
ENST00000673772.1:c.2667C>G	ENSP00000501168.1:p.Ile889Met
ENST00000673867.1:n.1048C>G
ENST00000674126.1:n.3264C>G
ENST00000674147.1:c.1836C>G	ENSP00000500964.1:p.Ile612Met
ENST00000242839.8:c.2901C>G	ENSP00000242839.4:p.Ile967Met
ENST00000344297.8:c.2280C>G	ENSP00000342559.5:p.Ile760Met
ENST00000400366.5:c.2568C>G	ENSP00000383217.3:p.Ile856Met
ENST00000400370.8:c.1611C>G	ENSP00000383221.3:p.Ile537Met
ENST00000418097.7:c.2866-2152C>G	ENSP00000393343.2:n.2866-2152C>G
ENST00000448424.6:c.2667C>G	ENSP00000416738.2:p.Ile889Met
ENST00000466629.1:n.121C>G
ENST00000634296.1:c.862C>G
ENST00000634308.1:c.*2C>G	ENSP00000489234.1:n.*2C>G
ENST00000634620.1:n.3645C>G
ENST00000634810.1:n.2246C>G
ENST00000634844.1:c.2757C>G	ENSP00000489398.1:p.Ile919Met
ENST00000635406.1:n.247C>G
NM_000053.3:c.2901C>G	NP_000044.2:p.Ile967Met
NM_001005918.2:c.2280C>G	NP_001005918.1:p.Ile760Met
NM_001243182.1:c.2568C>G	NP_001230111.1:p.Ile856Met
XM_005266423.2:c.2805C>G	XP_005266480.1:p.Ile935Met
XM_005266424.3:c.2805C>G	XP_005266481.1:p.Ile935Met
XM_005266427.2:c.2667C>G	XP_005266484.1:p.Ile889Met
XM_005266428.1:c.2649C>G	XP_005266485.1:p.Ile883Met
XM_005266430.3:c.2901C>G	XP_005266487.1:p.Ile967Met
XM_005266431.2:c.2865C>G	XP_005266488.1:p.Ile955Met
XM_005266432.2:c.2415C>G	XP_005266489.1:p.Ile805Met
XM_006719837.2:c.2805C>G	XP_006719900.1:p.Ile935Met
XM_006719838.1:c.717C>G	XP_006719901.1:p.Ile239Met
XM_006719839.1:c.717C>G	XP_006719902.1:p.Ile239Met
XM_011535117.1:c.2805C>G	XP_011533419.1:p.Ile935Met
XM_011535118.1:c.2766C>G	XP_011533420.1:p.Ile922Met
XM_011535119.1:c.2901C>G	XP_011533421.1:p.Ile967Met
XM_011535120.1:c.2487C>G	XP_011533422.1:p.Ile829Met
XM_011535121.1:c.2730+3564C>G	XP_011533423.1:n.2730+3564C>G
XM_011535122.1:c.1569C>G	XP_011533424.1:p.Ile523Met
XR_941601.1:n.3120C>G
XR_941602.1:n.3120C>G
XR_941603.1:n.3120C>G
XR_941604.1:n.3120C>G
NM_001330578.1:c.2667C>G	NP_001317507.1:p.Ile889Met
NM_001330579.1:c.2649C>G	NP_001317508.1:p.Ile883Met
XM_005266424.4:c.2805C>G	XP_005266481.1:p.Ile935Met
XM_005266430.4:c.2901C>G	XP_005266487.1:p.Ile967Met
XM_005266431.4:c.2865C>G	XP_005266488.1:p.Ile955Met
XM_006719837.3:c.2805C>G	XP_006719900.1:p.Ile935Met
XM_011535117.3:c.2805C>G	XP_011533419.1:p.Ile935Met
XM_017020627.1:c.2805C>G	XP_016876116.1:p.Ile935Met
NM_000053.4:c.2901C>G MANE Select	NP_000044.2:p.Ile967Met
NM_001005918.3:c.2280C>G	NP_001005918.1:p.Ile760Met
NM_001330579.2:c.2649C>G	NP_001317508.1:p.Ile883Met
NM_001243182.2:c.2568C>G	NP_001230111.1:p.Ile856Met
NM_001330578.2:c.2667C>G	NP_001317507.1:p.Ile889Met