Canonical Allele Identifier: CA388024060

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52513252T>G (hg19) ; chr13:g.51939116T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51939116T>G , CM000675.2:g.51939116T>G	GRCh38
NC_000013.10:g.52513252T>G , CM000675.1:g.52513252T>G	GRCh37
NC_000013.9:g.51411253T>G	NCBI36
NG_008806.1:g.77379A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1284A>C	ENSP00000489512.2:n.*1284A>C
ENST00000673864.2:c.*2378A>C	ENSP00000501045.2:n.*2378A>C
ENST00000674147.2:c.3013A>C	ENSP00000500964.2:p.Met1005Leu
ENST00000242839.10:c.3634A>C MANE Select	ENSP00000242839.5:p.Met1212Leu
ENST00000344297.9:c.3013A>C	ENSP00000342559.5:p.Met1005Leu
ENST00000400366.6:c.3301A>C	ENSP00000383217.3:p.Met1101Leu
ENST00000448424.7:c.3382A>C	ENSP00000416738.3:p.Met1128Leu
ENST00000673696.1:n.875A>C
ENST00000673772.1:c.3400A>C	ENSP00000501168.1:p.Met1134Leu
ENST00000673867.1:n.3773A>C
ENST00000673923.1:n.500A>C
ENST00000674147.1:c.2569A>C	ENSP00000500964.1:p.Met857Leu
ENST00000242839.8:c.3634A>C	ENSP00000242839.4:p.Met1212Leu
ENST00000344297.8:c.3013A>C	ENSP00000342559.5:p.Met1005Leu
ENST00000400366.5:c.3301A>C	ENSP00000383217.3:p.Met1101Leu
ENST00000400370.8:c.2344A>C	ENSP00000383221.3:p.Met782Leu
ENST00000418097.7:c.3439A>C	ENSP00000393343.2:p.Met1147Leu
ENST00000448424.6:c.3400A>C	ENSP00000416738.2:p.Met1134Leu
ENST00000634296.1:c.1412A>C
ENST00000634308.1:c.*735A>C	ENSP00000489234.1:n.*735A>C
ENST00000634620.1:n.4378A>C
ENST00000634810.1:n.2979A>C
ENST00000634844.1:c.3490A>C	ENSP00000489398.1:p.Met1164Leu
NM_000053.3:c.3634A>C	NP_000044.2:p.Met1212Leu
NM_001005918.2:c.3013A>C	NP_001005918.1:p.Met1005Leu
NM_001243182.1:c.3301A>C	NP_001230111.1:p.Met1101Leu
XM_005266423.2:c.3538A>C	XP_005266480.1:p.Met1180Leu
XM_005266424.3:c.3538A>C	XP_005266481.1:p.Met1180Leu
XM_005266427.2:c.3400A>C	XP_005266484.1:p.Met1134Leu
XM_005266428.1:c.3382A>C	XP_005266485.1:p.Met1128Leu
XM_005266430.3:c.3634A>C	XP_005266487.1:p.Met1212Leu
XM_005266431.2:c.3598A>C	XP_005266488.1:p.Met1200Leu
XM_005266432.2:c.3148A>C	XP_005266489.1:p.Met1050Leu
XM_006719837.2:c.3538A>C	XP_006719900.1:p.Met1180Leu
XM_006719838.1:c.1450A>C	XP_006719901.1:p.Met484Leu
XM_006719839.1:c.1267A>C	XP_006719902.1:p.Met423Leu
XM_011535117.1:c.3538A>C	XP_011533419.1:p.Met1180Leu
XM_011535118.1:c.3499A>C	XP_011533420.1:p.Met1167Leu
XM_011535119.1:c.3451A>C	XP_011533421.1:p.Met1151Leu
XM_011535120.1:c.3220A>C	XP_011533422.1:p.Met1074Leu
XM_011535121.1:c.3121A>C	XP_011533423.1:p.Met1041Leu
XM_011535122.1:c.2302A>C	XP_011533424.1:p.Met768Leu
XR_941601.1:n.3853A>C
XR_941602.1:n.3853A>C
XR_941603.1:n.3853A>C
XR_941604.1:n.3853A>C
NM_001330578.1:c.3400A>C	NP_001317507.1:p.Met1134Leu
NM_001330579.1:c.3382A>C	NP_001317508.1:p.Met1128Leu
XM_005266424.4:c.3538A>C	XP_005266481.1:p.Met1180Leu
XM_005266430.4:c.3634A>C	XP_005266487.1:p.Met1212Leu
XM_005266431.4:c.3598A>C	XP_005266488.1:p.Met1200Leu
XM_006719837.3:c.3538A>C	XP_006719900.1:p.Met1180Leu
XM_011535117.3:c.3538A>C	XP_011533419.1:p.Met1180Leu
XM_017020627.1:c.3538A>C	XP_016876116.1:p.Met1180Leu
NM_000053.4:c.3634A>C MANE Select	NP_000044.2:p.Met1212Leu
NM_001005918.3:c.3013A>C	NP_001005918.1:p.Met1005Leu
NM_001330579.2:c.3382A>C	NP_001317508.1:p.Met1128Leu
NM_001243182.2:c.3301A>C	NP_001230111.1:p.Met1101Leu
NM_001330578.2:c.3400A>C	NP_001317507.1:p.Met1134Leu