Canonical Allele Identifier: CA388034863

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52524271G>C (hg19) ; chr13:g.51950135G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51950135G>C , CM000675.2:g.51950135G>C	GRCh38
NC_000013.10:g.52524271G>C , CM000675.1:g.52524271G>C	GRCh37
NC_000013.9:g.51422272G>C	NCBI36
NG_008806.1:g.66360C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*435C>G	ENSP00000489512.2:n.*435C>G
ENST00000673864.2:c.*1346C>G	ENSP00000501045.2:n.*1346C>G
ENST00000674147.2:c.2116C>G	ENSP00000500964.2:p.Pro706Ala
ENST00000242839.10:c.2602C>G MANE Select	ENSP00000242839.5:p.Pro868Ala
ENST00000344297.9:c.2116C>G	ENSP00000342559.5:p.Pro706Ala
ENST00000400366.6:c.2269C>G	ENSP00000383217.3:p.Pro757Ala
ENST00000448424.7:c.2350C>G	ENSP00000416738.3:p.Pro784Ala
ENST00000673772.1:c.2368C>G	ENSP00000501168.1:p.Pro790Ala
ENST00000674147.1:c.1672C>G	ENSP00000500964.1:p.Pro558Ala
ENST00000242839.8:c.2602C>G	ENSP00000242839.4:p.Pro868Ala
ENST00000344297.8:c.2116C>G	ENSP00000342559.5:p.Pro706Ala
ENST00000400366.5:c.2269C>G	ENSP00000383217.3:p.Pro757Ala
ENST00000400370.8:c.1312C>G	ENSP00000383221.3:p.Pro438Ala
ENST00000418097.7:c.2602C>G	ENSP00000393343.2:p.Pro868Ala
ENST00000448424.6:c.2368C>G	ENSP00000416738.2:p.Pro790Ala
ENST00000634296.1:c.563C>G
ENST00000634308.1:c.2368C>G	ENSP00000489234.1:p.Pro790Ala
ENST00000634620.1:n.3400C>G
ENST00000634810.1:n.1947C>G
ENST00000634844.1:c.2458C>G	ENSP00000489398.1:p.Pro820Ala
ENST00000635406.1:n.212-3657C>G
NM_000053.3:c.2602C>G	NP_000044.2:p.Pro868Ala
NM_001005918.2:c.2116C>G	NP_001005918.1:p.Pro706Ala
NM_001243182.1:c.2269C>G	NP_001230111.1:p.Pro757Ala
XM_005266423.2:c.2506C>G	XP_005266480.1:p.Pro836Ala
XM_005266424.3:c.2506C>G	XP_005266481.1:p.Pro836Ala
XM_005266427.2:c.2368C>G	XP_005266484.1:p.Pro790Ala
XM_005266428.1:c.2350C>G	XP_005266485.1:p.Pro784Ala
XM_005266430.3:c.2602C>G	XP_005266487.1:p.Pro868Ala
XM_005266431.2:c.2566C>G	XP_005266488.1:p.Pro856Ala
XM_005266432.2:c.2116C>G	XP_005266489.1:p.Pro706Ala
XM_006719837.2:c.2506C>G	XP_006719900.1:p.Pro836Ala
XM_006719838.1:c.418C>G	XP_006719901.1:p.Pro140Ala
XM_006719839.1:c.418C>G	XP_006719902.1:p.Pro140Ala
XM_011535117.1:c.2506C>G	XP_011533419.1:p.Pro836Ala
XM_011535118.1:c.2602C>G	XP_011533420.1:p.Pro868Ala
XM_011535119.1:c.2602C>G	XP_011533421.1:p.Pro868Ala
XM_011535120.1:c.2188C>G	XP_011533422.1:p.Pro730Ala
XM_011535121.1:c.2602C>G	XP_011533423.1:p.Pro868Ala
XM_011535122.1:c.1270C>G	XP_011533424.1:p.Pro424Ala
XR_941601.1:n.2821C>G
XR_941602.1:n.2821C>G
XR_941603.1:n.2821C>G
XR_941604.1:n.2821C>G
NM_001330578.1:c.2368C>G	NP_001317507.1:p.Pro790Ala
NM_001330579.1:c.2350C>G	NP_001317508.1:p.Pro784Ala
XM_005266424.4:c.2506C>G	XP_005266481.1:p.Pro836Ala
XM_005266430.4:c.2602C>G	XP_005266487.1:p.Pro868Ala
XM_005266431.4:c.2566C>G	XP_005266488.1:p.Pro856Ala
XM_006719837.3:c.2506C>G	XP_006719900.1:p.Pro836Ala
XM_011535117.3:c.2506C>G	XP_011533419.1:p.Pro836Ala
XM_017020627.1:c.2506C>G	XP_016876116.1:p.Pro836Ala
NM_000053.4:c.2602C>G MANE Select	NP_000044.2:p.Pro868Ala
NM_001005918.3:c.2116C>G	NP_001005918.1:p.Pro706Ala
NM_001330579.2:c.2350C>G	NP_001317508.1:p.Pro784Ala
NM_001243182.2:c.2269C>G	NP_001230111.1:p.Pro757Ala
NM_001330578.2:c.2368C>G	NP_001317507.1:p.Pro790Ala