Canonical Allele Identifier: CA388032027
Community Standard Title: NM_000053.4(ATP7B):c.3007G>C (p.Ala1003Pro)
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51946337C>G , CM000675.2:g.51946337C>G GRCh38
NC_000013.10:g.52520473C>G , CM000675.1:g.52520473C>G GRCh37
NC_000013.9:g.51418474C>G NCBI36
NG_008806.1:g.70158G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000053.4:c.3007G>C MANE Select NP_000044.2:p.Ala1003Pro
ENST00000242839.10:c.3007G>C MANE Select ENSP00000242839.5:p.Ala1003Pro
NM_000053.3:c.3007G>C NP_000044.2:p.Ala1003Pro
NM_001005918.2:c.2386G>C NP_001005918.1:p.Ala796Pro
NM_001005918.3:c.2386G>C NP_001005918.1:p.Ala796Pro
NM_001243182.1:c.2674G>C NP_001230111.1:p.Ala892Pro
NM_001243182.2:c.2674G>C NP_001230111.1:p.Ala892Pro
NM_001330578.1:c.2773G>C NP_001317507.1:p.Ala925Pro
NM_001330578.2:c.2773G>C NP_001317507.1:p.Ala925Pro
NM_001330579.1:c.2755G>C NP_001317508.1:p.Ala919Pro
NM_001330579.2:c.2755G>C NP_001317508.1:p.Ala919Pro
ENST00000242839.8:c.3007G>C ENSP00000242839.4:p.Ala1003Pro
ENST00000344297.8:c.2386G>C ENSP00000342559.5:p.Ala796Pro
ENST00000344297.9:c.2386G>C ENSP00000342559.5:p.Ala796Pro
ENST00000400366.5:c.2674G>C ENSP00000383217.3:p.Ala892Pro
ENST00000400366.6:c.2674G>C ENSP00000383217.3:p.Ala892Pro
ENST00000400370.8:c.1717G>C ENSP00000383221.3:p.Ala573Pro
ENST00000418097.7:c.2866-2046G>C ENSP00000393343.2:n.2866-2046G>C
ENST00000448424.6:c.2773G>C ENSP00000416738.2:p.Ala925Pro
ENST00000448424.7:c.2755G>C ENSP00000416738.3:p.Ala919Pro
ENST00000466629.1:n.227G>C
ENST00000634296.1:c.968G>C
ENST00000634296.2:c.*840G>C ENSP00000489512.2:n.*840G>C
ENST00000634308.1:c.*108G>C ENSP00000489234.1:n.*108G>C
ENST00000634620.1:n.3751G>C
ENST00000634810.1:n.2352G>C
ENST00000634844.1:c.2863G>C ENSP00000489398.1:p.Ala955Pro
ENST00000635406.1:n.353G>C
ENST00000673772.1:c.2773G>C ENSP00000501168.1:p.Ala925Pro
ENST00000673864.2:c.*1751G>C ENSP00000501045.2:n.*1751G>C
ENST00000673867.1:n.1154G>C
ENST00000674126.1:n.3370G>C
ENST00000674147.1:c.1942G>C ENSP00000500964.1:p.Ala648Pro
ENST00000674147.2:c.2386G>C ENSP00000500964.2:p.Ala796Pro
XM_005266423.2:c.2911G>C XP_005266480.1:p.Ala971Pro
XM_005266424.3:c.2911G>C XP_005266481.1:p.Ala971Pro
XM_005266424.4:c.2911G>C XP_005266481.1:p.Ala971Pro
XM_005266427.2:c.2773G>C XP_005266484.1:p.Ala925Pro
XM_005266428.1:c.2755G>C XP_005266485.1:p.Ala919Pro
XM_005266430.3:c.3007G>C XP_005266487.1:p.Ala1003Pro
XM_005266430.4:c.3007G>C XP_005266487.1:p.Ala1003Pro
XM_005266431.2:c.2971G>C XP_005266488.1:p.Ala991Pro
XM_005266431.4:c.2971G>C XP_005266488.1:p.Ala991Pro
XM_005266432.2:c.2521G>C XP_005266489.1:p.Ala841Pro
XM_006719837.2:c.2911G>C XP_006719900.1:p.Ala971Pro
XM_006719837.3:c.2911G>C XP_006719900.1:p.Ala971Pro
XM_006719838.1:c.823G>C XP_006719901.1:p.Ala275Pro
XM_006719839.1:c.823G>C XP_006719902.1:p.Ala275Pro
XM_011535117.1:c.2911G>C XP_011533419.1:p.Ala971Pro
XM_011535117.3:c.2911G>C XP_011533419.1:p.Ala971Pro
XM_011535118.1:c.2872G>C XP_011533420.1:p.Ala958Pro
XM_011535119.1:c.3007G>C XP_011533421.1:p.Ala1003Pro
XM_011535120.1:c.2593G>C XP_011533422.1:p.Ala865Pro
XM_011535121.1:c.2730+3670G>C XP_011533423.1:n.2730+3670G>C
XM_011535122.1:c.1675G>C XP_011533424.1:p.Ala559Pro
XM_017020627.1:c.2911G>C XP_016876116.1:p.Ala971Pro
XR_941601.1:n.3226G>C
XR_941602.1:n.3226G>C
XR_941603.1:n.3226G>C
XR_941604.1:n.3226G>C