Canonical Allele Identifier: CA388032023

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 3075300
• ClinVar RCV Id: RCV004015826
• gnomAD v4: 13-51946336-G-C
• MyVariant Identifiers: chr13:g.52520472G>C (hg19) ; chr13:g.51946336G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946336G>C , CM000675.2:g.51946336G>C	GRCh38
NC_000013.10:g.52520472G>C , CM000675.1:g.52520472G>C	GRCh37
NC_000013.9:g.51418473G>C	NCBI36
NG_008806.1:g.70159C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*841C>G	ENSP00000489512.2:n.*841C>G
ENST00000673864.2:c.*1752C>G	ENSP00000501045.2:n.*1752C>G
ENST00000674147.2:c.2387C>G	ENSP00000500964.2:p.Ala796Gly
ENST00000242839.10:c.3008C>G MANE Select	ENSP00000242839.5:p.Ala1003Gly
ENST00000344297.9:c.2387C>G	ENSP00000342559.5:p.Ala796Gly
ENST00000400366.6:c.2675C>G	ENSP00000383217.3:p.Ala892Gly
ENST00000448424.7:c.2756C>G	ENSP00000416738.3:p.Ala919Gly
ENST00000673772.1:c.2774C>G	ENSP00000501168.1:p.Ala925Gly
ENST00000673867.1:n.1155C>G
ENST00000674126.1:n.3371C>G
ENST00000674147.1:c.1943C>G	ENSP00000500964.1:p.Ala648Gly
ENST00000242839.8:c.3008C>G	ENSP00000242839.4:p.Ala1003Gly
ENST00000344297.8:c.2387C>G	ENSP00000342559.5:p.Ala796Gly
ENST00000400366.5:c.2675C>G	ENSP00000383217.3:p.Ala892Gly
ENST00000400370.8:c.1718C>G	ENSP00000383221.3:p.Ala573Gly
ENST00000418097.7:c.2866-2045C>G	ENSP00000393343.2:n.2866-2045C>G
ENST00000448424.6:c.2774C>G	ENSP00000416738.2:p.Ala925Gly
ENST00000466629.1:n.228C>G
ENST00000634296.1:c.969C>G
ENST00000634308.1:c.*109C>G	ENSP00000489234.1:n.*109C>G
ENST00000634620.1:n.3752C>G
ENST00000634810.1:n.2353C>G
ENST00000634844.1:c.2864C>G	ENSP00000489398.1:p.Ala955Gly
ENST00000635406.1:n.354C>G
NM_000053.3:c.3008C>G	NP_000044.2:p.Ala1003Gly
NM_001005918.2:c.2387C>G	NP_001005918.1:p.Ala796Gly
NM_001243182.1:c.2675C>G	NP_001230111.1:p.Ala892Gly
XM_005266423.2:c.2912C>G	XP_005266480.1:p.Ala971Gly
XM_005266424.3:c.2912C>G	XP_005266481.1:p.Ala971Gly
XM_005266427.2:c.2774C>G	XP_005266484.1:p.Ala925Gly
XM_005266428.1:c.2756C>G	XP_005266485.1:p.Ala919Gly
XM_005266430.3:c.3008C>G	XP_005266487.1:p.Ala1003Gly
XM_005266431.2:c.2972C>G	XP_005266488.1:p.Ala991Gly
XM_005266432.2:c.2522C>G	XP_005266489.1:p.Ala841Gly
XM_006719837.2:c.2912C>G	XP_006719900.1:p.Ala971Gly
XM_006719838.1:c.824C>G	XP_006719901.1:p.Ala275Gly
XM_006719839.1:c.824C>G	XP_006719902.1:p.Ala275Gly
XM_011535117.1:c.2912C>G	XP_011533419.1:p.Ala971Gly
XM_011535118.1:c.2873C>G	XP_011533420.1:p.Ala958Gly
XM_011535119.1:c.3008C>G	XP_011533421.1:p.Ala1003Gly
XM_011535120.1:c.2594C>G	XP_011533422.1:p.Ala865Gly
XM_011535121.1:c.2730+3671C>G	XP_011533423.1:n.2730+3671C>G
XM_011535122.1:c.1676C>G	XP_011533424.1:p.Ala559Gly
XR_941601.1:n.3227C>G
XR_941602.1:n.3227C>G
XR_941603.1:n.3227C>G
XR_941604.1:n.3227C>G
NM_001330578.1:c.2774C>G	NP_001317507.1:p.Ala925Gly
NM_001330579.1:c.2756C>G	NP_001317508.1:p.Ala919Gly
XM_005266424.4:c.2912C>G	XP_005266481.1:p.Ala971Gly
XM_005266430.4:c.3008C>G	XP_005266487.1:p.Ala1003Gly
XM_005266431.4:c.2972C>G	XP_005266488.1:p.Ala991Gly
XM_006719837.3:c.2912C>G	XP_006719900.1:p.Ala971Gly
XM_011535117.3:c.2912C>G	XP_011533419.1:p.Ala971Gly
XM_017020627.1:c.2912C>G	XP_016876116.1:p.Ala971Gly
NM_000053.4:c.3008C>G MANE Select	NP_000044.2:p.Ala1003Gly
NM_001005918.3:c.2387C>G	NP_001005918.1:p.Ala796Gly
NM_001330579.2:c.2756C>G	NP_001317508.1:p.Ala919Gly
NM_001243182.2:c.2675C>G	NP_001230111.1:p.Ala892Gly
NM_001330578.2:c.2774C>G	NP_001317507.1:p.Ala925Gly