Canonical Allele Identifier: CA388024688

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52513314A>T (hg19) ; chr13:g.51939178A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51939178A>T , CM000675.2:g.51939178A>T	GRCh38
NC_000013.10:g.52513314A>T , CM000675.1:g.52513314A>T	GRCh37
NC_000013.9:g.51411315A>T	NCBI36
NG_008806.1:g.77317T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1222T>A	ENSP00000489512.2:n.*1222T>A
ENST00000673864.2:c.*2316T>A	ENSP00000501045.2:n.*2316T>A
ENST00000674147.2:c.2951T>A	ENSP00000500964.2:p.Met984Lys
ENST00000242839.10:c.3572T>A MANE Select	ENSP00000242839.5:p.Met1191Lys
ENST00000344297.9:c.2951T>A	ENSP00000342559.5:p.Met984Lys
ENST00000400366.6:c.3239T>A	ENSP00000383217.3:p.Met1080Lys
ENST00000448424.7:c.3320T>A	ENSP00000416738.3:p.Met1107Lys
ENST00000673696.1:n.813T>A
ENST00000673772.1:c.3338T>A	ENSP00000501168.1:p.Met1113Lys
ENST00000673867.1:n.3711T>A
ENST00000673923.1:n.438T>A
ENST00000674147.1:c.2507T>A	ENSP00000500964.1:p.Met836Lys
ENST00000242839.8:c.3572T>A	ENSP00000242839.4:p.Met1191Lys
ENST00000344297.8:c.2951T>A	ENSP00000342559.5:p.Met984Lys
ENST00000400366.5:c.3239T>A	ENSP00000383217.3:p.Met1080Lys
ENST00000400370.8:c.2282T>A	ENSP00000383221.3:p.Met761Lys
ENST00000418097.7:c.3377T>A	ENSP00000393343.2:p.Met1126Lys
ENST00000448424.6:c.3338T>A	ENSP00000416738.2:p.Met1113Lys
ENST00000634296.1:c.1350T>A
ENST00000634308.1:c.*673T>A	ENSP00000489234.1:n.*673T>A
ENST00000634620.1:n.4316T>A
ENST00000634810.1:n.2917T>A
ENST00000634844.1:c.3428T>A	ENSP00000489398.1:p.Met1143Lys
NM_000053.3:c.3572T>A	NP_000044.2:p.Met1191Lys
NM_001005918.2:c.2951T>A	NP_001005918.1:p.Met984Lys
NM_001243182.1:c.3239T>A	NP_001230111.1:p.Met1080Lys
XM_005266423.2:c.3476T>A	XP_005266480.1:p.Met1159Lys
XM_005266424.3:c.3476T>A	XP_005266481.1:p.Met1159Lys
XM_005266427.2:c.3338T>A	XP_005266484.1:p.Met1113Lys
XM_005266428.1:c.3320T>A	XP_005266485.1:p.Met1107Lys
XM_005266430.3:c.3572T>A	XP_005266487.1:p.Met1191Lys
XM_005266431.2:c.3536T>A	XP_005266488.1:p.Met1179Lys
XM_005266432.2:c.3086T>A	XP_005266489.1:p.Met1029Lys
XM_006719837.2:c.3476T>A	XP_006719900.1:p.Met1159Lys
XM_006719838.1:c.1388T>A	XP_006719901.1:p.Met463Lys
XM_006719839.1:c.1205T>A	XP_006719902.1:p.Met402Lys
XM_011535117.1:c.3476T>A	XP_011533419.1:p.Met1159Lys
XM_011535118.1:c.3437T>A	XP_011533420.1:p.Met1146Lys
XM_011535119.1:c.3389T>A	XP_011533421.1:p.Met1130Lys
XM_011535120.1:c.3158T>A	XP_011533422.1:p.Met1053Lys
XM_011535121.1:c.3059T>A	XP_011533423.1:p.Met1020Lys
XM_011535122.1:c.2240T>A	XP_011533424.1:p.Met747Lys
XR_941601.1:n.3791T>A
XR_941602.1:n.3791T>A
XR_941603.1:n.3791T>A
XR_941604.1:n.3791T>A
NM_001330578.1:c.3338T>A	NP_001317507.1:p.Met1113Lys
NM_001330579.1:c.3320T>A	NP_001317508.1:p.Met1107Lys
XM_005266424.4:c.3476T>A	XP_005266481.1:p.Met1159Lys
XM_005266430.4:c.3572T>A	XP_005266487.1:p.Met1191Lys
XM_005266431.4:c.3536T>A	XP_005266488.1:p.Met1179Lys
XM_006719837.3:c.3476T>A	XP_006719900.1:p.Met1159Lys
XM_011535117.3:c.3476T>A	XP_011533419.1:p.Met1159Lys
XM_017020627.1:c.3476T>A	XP_016876116.1:p.Met1159Lys
NM_000053.4:c.3572T>A MANE Select	NP_000044.2:p.Met1191Lys
NM_001005918.3:c.2951T>A	NP_001005918.1:p.Met984Lys
NM_001330579.2:c.3320T>A	NP_001317508.1:p.Met1107Lys
NM_001243182.2:c.3239T>A	NP_001230111.1:p.Met1080Lys
NM_001330578.2:c.3338T>A	NP_001317507.1:p.Met1113Lys