Canonical Allele Identifier: CA388030324

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52518369A>G (hg19) ; chr13:g.51944233A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944233A>G , CM000675.2:g.51944233A>G	GRCh38
NC_000013.10:g.52518369A>G , CM000675.1:g.52518369A>G	GRCh37
NC_000013.9:g.51416370A>G	NCBI36
NG_008806.1:g.72262T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*894-1679T>C	ENSP00000489512.2:n.*894-1679T>C
ENST00000673864.2:c.*1863T>C	ENSP00000501045.2:n.*1863T>C
ENST00000674147.2:c.2498T>C	ENSP00000500964.2:p.Met833Thr
ENST00000242839.10:c.3119T>C MANE Select	ENSP00000242839.5:p.Met1040Thr
ENST00000344297.9:c.2498T>C	ENSP00000342559.5:p.Met833Thr
ENST00000400366.6:c.2786T>C	ENSP00000383217.3:p.Met929Thr
ENST00000448424.7:c.2867T>C	ENSP00000416738.3:p.Met956Thr
ENST00000673772.1:c.2885T>C	ENSP00000501168.1:p.Met962Thr
ENST00000673867.1:n.3258T>C
ENST00000674126.1:n.3482T>C
ENST00000674147.1:c.2054T>C	ENSP00000500964.1:p.Met685Thr
ENST00000242839.8:c.3119T>C	ENSP00000242839.4:p.Met1040Thr
ENST00000344297.8:c.2498T>C	ENSP00000342559.5:p.Met833Thr
ENST00000400366.5:c.2786T>C	ENSP00000383217.3:p.Met929Thr
ENST00000400370.8:c.1829T>C	ENSP00000383221.3:p.Met610Thr
ENST00000418097.7:c.2924T>C	ENSP00000393343.2:p.Met975Thr
ENST00000448424.6:c.2885T>C	ENSP00000416738.2:p.Met962Thr
ENST00000466629.1:n.339T>C
ENST00000634296.1:c.1022-1679T>C
ENST00000634308.1:c.*220T>C	ENSP00000489234.1:n.*220T>C
ENST00000634620.1:n.3863T>C
ENST00000634810.1:n.2464T>C
ENST00000634844.1:c.2975T>C	ENSP00000489398.1:p.Met992Thr
ENST00000635406.1:n.465T>C
NM_000053.3:c.3119T>C	NP_000044.2:p.Met1040Thr
NM_001005918.2:c.2498T>C	NP_001005918.1:p.Met833Thr
NM_001243182.1:c.2786T>C	NP_001230111.1:p.Met929Thr
XM_005266423.2:c.3023T>C	XP_005266480.1:p.Met1008Thr
XM_005266424.3:c.3023T>C	XP_005266481.1:p.Met1008Thr
XM_005266427.2:c.2885T>C	XP_005266484.1:p.Met962Thr
XM_005266428.1:c.2867T>C	XP_005266485.1:p.Met956Thr
XM_005266430.3:c.3119T>C	XP_005266487.1:p.Met1040Thr
XM_005266431.2:c.3083T>C	XP_005266488.1:p.Met1028Thr
XM_005266432.2:c.2633T>C	XP_005266489.1:p.Met878Thr
XM_006719837.2:c.3023T>C	XP_006719900.1:p.Met1008Thr
XM_006719838.1:c.935T>C	XP_006719901.1:p.Met312Thr
XM_006719839.1:c.877-1679T>C	XP_006719902.1:n.877-1679T>C
XM_011535117.1:c.3023T>C	XP_011533419.1:p.Met1008Thr
XM_011535118.1:c.2984T>C	XP_011533420.1:p.Met995Thr
XM_011535119.1:c.3061-1679T>C	XP_011533421.1:n.3061-1679T>C
XM_011535120.1:c.2705T>C	XP_011533422.1:p.Met902Thr
XM_011535121.1:c.2731-1679T>C	XP_011533423.1:n.2731-1679T>C
XM_011535122.1:c.1787T>C	XP_011533424.1:p.Met596Thr
XR_941601.1:n.3338T>C
XR_941602.1:n.3338T>C
XR_941603.1:n.3338T>C
XR_941604.1:n.3338T>C
NM_001330578.1:c.2885T>C	NP_001317507.1:p.Met962Thr
NM_001330579.1:c.2867T>C	NP_001317508.1:p.Met956Thr
XM_005266424.4:c.3023T>C	XP_005266481.1:p.Met1008Thr
XM_005266430.4:c.3119T>C	XP_005266487.1:p.Met1040Thr
XM_005266431.4:c.3083T>C	XP_005266488.1:p.Met1028Thr
XM_006719837.3:c.3023T>C	XP_006719900.1:p.Met1008Thr
XM_011535117.3:c.3023T>C	XP_011533419.1:p.Met1008Thr
XM_017020627.1:c.3023T>C	XP_016876116.1:p.Met1008Thr
NM_000053.4:c.3119T>C MANE Select	NP_000044.2:p.Met1040Thr
NM_001005918.3:c.2498T>C	NP_001005918.1:p.Met833Thr
NM_001330579.2:c.2867T>C	NP_001317508.1:p.Met956Thr
NM_001243182.2:c.2786T>C	NP_001230111.1:p.Met929Thr
NM_001330578.2:c.2885T>C	NP_001317507.1:p.Met962Thr