Canonical Allele Identifier: CA388029876

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52518281G>C (hg19) ; chr13:g.51944145G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944145G>C , CM000675.2:g.51944145G>C	GRCh38
NC_000013.10:g.52518281G>C , CM000675.1:g.52518281G>C	GRCh37
NC_000013.9:g.51416282G>C	NCBI36
NG_008806.1:g.72350C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1591C>G	ENSP00000489512.2:n.*894-1591C>G
ENST00000673864.2:c.*1951C>G	ENSP00000501045.2:n.*1951C>G
ENST00000674147.2:c.2586C>G	ENSP00000500964.2:p.His862Gln
ENST00000242839.10:c.3207C>G MANE Select	ENSP00000242839.5:p.His1069Gln
ENST00000344297.9:c.2586C>G	ENSP00000342559.5:p.His862Gln
ENST00000400366.6:c.2874C>G	ENSP00000383217.3:p.His958Gln
ENST00000448424.7:c.2955C>G	ENSP00000416738.3:p.His985Gln
ENST00000673772.1:c.2973C>G	ENSP00000501168.1:p.His991Gln
ENST00000673867.1:n.3346C>G
ENST00000674126.1:n.3570C>G
ENST00000674147.1:c.2142C>G	ENSP00000500964.1:p.His714Gln
ENST00000242839.8:c.3207C>G	ENSP00000242839.4:p.His1069Gln
ENST00000344297.8:c.2586C>G	ENSP00000342559.5:p.His862Gln
ENST00000400366.5:c.2874C>G	ENSP00000383217.3:p.His958Gln
ENST00000400370.8:c.1917C>G	ENSP00000383221.3:p.His639Gln
ENST00000418097.7:c.3012C>G	ENSP00000393343.2:p.His1004Gln
ENST00000448424.6:c.2973C>G	ENSP00000416738.2:p.His991Gln
ENST00000466629.1:n.427C>G
ENST00000634296.1:c.1022-1591C>G
ENST00000634308.1:c.*308C>G	ENSP00000489234.1:n.*308C>G
ENST00000634620.1:n.3951C>G
ENST00000634810.1:n.2552C>G
ENST00000634844.1:c.3063C>G	ENSP00000489398.1:p.His1021Gln
NM_000053.3:c.3207C>G	NP_000044.2:p.His1069Gln
NM_001005918.2:c.2586C>G	NP_001005918.1:p.His862Gln
NM_001243182.1:c.2874C>G	NP_001230111.1:p.His958Gln
XM_005266423.2:c.3111C>G	XP_005266480.1:p.His1037Gln
XM_005266424.3:c.3111C>G	XP_005266481.1:p.His1037Gln
XM_005266427.2:c.2973C>G	XP_005266484.1:p.His991Gln
XM_005266428.1:c.2955C>G	XP_005266485.1:p.His985Gln
XM_005266430.3:c.3207C>G	XP_005266487.1:p.His1069Gln
XM_005266431.2:c.3171C>G	XP_005266488.1:p.His1057Gln
XM_005266432.2:c.2721C>G	XP_005266489.1:p.His907Gln
XM_006719837.2:c.3111C>G	XP_006719900.1:p.His1037Gln
XM_006719838.1:c.1023C>G	XP_006719901.1:p.His341Gln
XM_006719839.1:c.877-1591C>G	XP_006719902.1:n.877-1591C>G
XM_011535117.1:c.3111C>G	XP_011533419.1:p.His1037Gln
XM_011535118.1:c.3072C>G	XP_011533420.1:p.His1024Gln
XM_011535119.1:c.3061-1591C>G	XP_011533421.1:n.3061-1591C>G
XM_011535120.1:c.2793C>G	XP_011533422.1:p.His931Gln
XM_011535121.1:c.2731-1591C>G	XP_011533423.1:n.2731-1591C>G
XM_011535122.1:c.1875C>G	XP_011533424.1:p.His625Gln
XR_941601.1:n.3426C>G
XR_941602.1:n.3426C>G
XR_941603.1:n.3426C>G
XR_941604.1:n.3426C>G
NM_001330578.1:c.2973C>G	NP_001317507.1:p.His991Gln
NM_001330579.1:c.2955C>G	NP_001317508.1:p.His985Gln
XM_005266424.4:c.3111C>G	XP_005266481.1:p.His1037Gln
XM_005266430.4:c.3207C>G	XP_005266487.1:p.His1069Gln
XM_005266431.4:c.3171C>G	XP_005266488.1:p.His1057Gln
XM_006719837.3:c.3111C>G	XP_006719900.1:p.His1037Gln
XM_011535117.3:c.3111C>G	XP_011533419.1:p.His1037Gln
XM_017020627.1:c.3111C>G	XP_016876116.1:p.His1037Gln
NM_000053.4:c.3207C>G MANE Select	NP_000044.2:p.His1069Gln
NM_001005918.3:c.2586C>G	NP_001005918.1:p.His862Gln
NM_001330579.2:c.2955C>G	NP_001317508.1:p.His985Gln
NM_001243182.2:c.2874C>G	NP_001230111.1:p.His958Gln
NM_001330578.2:c.2973C>G	NP_001317507.1:p.His991Gln