Canonical Allele Identifier: CA388026139

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515253T>G (hg19) ; chr13:g.51941117T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941117T>G , CM000675.2:g.51941117T>G	GRCh38
NC_000013.10:g.52515253T>G , CM000675.1:g.52515253T>G	GRCh37
NC_000013.9:g.51413254T>G	NCBI36
NG_008806.1:g.75378A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1170A>C	ENSP00000489512.2:n.*1170A>C
ENST00000673864.2:c.*2264A>C	ENSP00000501045.2:n.*2264A>C
ENST00000674147.2:c.2899A>C	ENSP00000500964.2:p.Met967Leu
ENST00000242839.10:c.3520A>C MANE Select	ENSP00000242839.5:p.Met1174Leu
ENST00000344297.9:c.2899A>C	ENSP00000342559.5:p.Met967Leu
ENST00000400366.6:c.3187A>C	ENSP00000383217.3:p.Met1063Leu
ENST00000448424.7:c.3268A>C	ENSP00000416738.3:p.Met1090Leu
ENST00000673772.1:c.3286A>C	ENSP00000501168.1:p.Met1096Leu
ENST00000673867.1:n.3659A>C
ENST00000674126.1:n.3883A>C
ENST00000674147.1:c.2455A>C	ENSP00000500964.1:p.Met819Leu
ENST00000242839.8:c.3520A>C	ENSP00000242839.4:p.Met1174Leu
ENST00000344297.8:c.2899A>C	ENSP00000342559.5:p.Met967Leu
ENST00000400366.5:c.3187A>C	ENSP00000383217.3:p.Met1063Leu
ENST00000400370.8:c.2230A>C	ENSP00000383221.3:p.Met744Leu
ENST00000418097.7:c.3325A>C	ENSP00000393343.2:p.Met1109Leu
ENST00000448424.6:c.3286A>C	ENSP00000416738.2:p.Met1096Leu
ENST00000634296.1:c.1298A>C
ENST00000634308.1:c.*621A>C	ENSP00000489234.1:n.*621A>C
ENST00000634620.1:n.4264A>C
ENST00000634810.1:n.2865A>C
ENST00000634844.1:c.3376A>C	ENSP00000489398.1:p.Met1126Leu
NM_000053.3:c.3520A>C	NP_000044.2:p.Met1174Leu
NM_001005918.2:c.2899A>C	NP_001005918.1:p.Met967Leu
NM_001243182.1:c.3187A>C	NP_001230111.1:p.Met1063Leu
XM_005266423.2:c.3424A>C	XP_005266480.1:p.Met1142Leu
XM_005266424.3:c.3424A>C	XP_005266481.1:p.Met1142Leu
XM_005266427.2:c.3286A>C	XP_005266484.1:p.Met1096Leu
XM_005266428.1:c.3268A>C	XP_005266485.1:p.Met1090Leu
XM_005266430.3:c.3520A>C	XP_005266487.1:p.Met1174Leu
XM_005266431.2:c.3484A>C	XP_005266488.1:p.Met1162Leu
XM_005266432.2:c.3034A>C	XP_005266489.1:p.Met1012Leu
XM_006719837.2:c.3424A>C	XP_006719900.1:p.Met1142Leu
XM_006719838.1:c.1336A>C	XP_006719901.1:p.Met446Leu
XM_006719839.1:c.1153A>C	XP_006719902.1:p.Met385Leu
XM_011535117.1:c.3424A>C	XP_011533419.1:p.Met1142Leu
XM_011535118.1:c.3385A>C	XP_011533420.1:p.Met1129Leu
XM_011535119.1:c.3337A>C	XP_011533421.1:p.Met1113Leu
XM_011535120.1:c.3106A>C	XP_011533422.1:p.Met1036Leu
XM_011535121.1:c.3007A>C	XP_011533423.1:p.Met1003Leu
XM_011535122.1:c.2188A>C	XP_011533424.1:p.Met730Leu
XR_941601.1:n.3739A>C
XR_941602.1:n.3739A>C
XR_941603.1:n.3739A>C
XR_941604.1:n.3739A>C
NM_001330578.1:c.3286A>C	NP_001317507.1:p.Met1096Leu
NM_001330579.1:c.3268A>C	NP_001317508.1:p.Met1090Leu
XM_005266424.4:c.3424A>C	XP_005266481.1:p.Met1142Leu
XM_005266430.4:c.3520A>C	XP_005266487.1:p.Met1174Leu
XM_005266431.4:c.3484A>C	XP_005266488.1:p.Met1162Leu
XM_006719837.3:c.3424A>C	XP_006719900.1:p.Met1142Leu
XM_011535117.3:c.3424A>C	XP_011533419.1:p.Met1142Leu
XM_017020627.1:c.3424A>C	XP_016876116.1:p.Met1142Leu
NM_000053.4:c.3520A>C MANE Select	NP_000044.2:p.Met1174Leu
NM_001005918.3:c.2899A>C	NP_001005918.1:p.Met967Leu
NM_001330579.2:c.3268A>C	NP_001317508.1:p.Met1090Leu
NM_001243182.2:c.3187A>C	NP_001230111.1:p.Met1063Leu
NM_001330578.2:c.3286A>C	NP_001317507.1:p.Met1096Leu