Canonical Allele Identifier: CA413605939
Community Standard Title: NM_000052.7(ATP7A):c.4223A>C (p.Lys1408Thr)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78045569A>C , CM000685.2:g.78045569A>C GRCh38
NC_000023.10:g.77301066A>C , CM000685.1:g.77301066A>C GRCh37
NC_000023.9:g.77187722A>C NCBI36
NG_013224.2:g.139873A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000052.7:c.4223A>C (ATP7A) MANE Select NP_000043.4:p.Lys1408Thr
ENST00000341514.11:c.4223A>C (ATP7A) MANE Select ENSP00000345728.6:p.Lys1408Thr
NM_000052.6:c.4223A>C (ATP7A) NP_000043.4:p.Lys1408Thr
NM_001282224.1:c.3989A>C (ATP7A) NP_001269153.1:p.Lys1330Thr
NM_001282224.2:c.3989A>C (ATP7A) NP_001269153.1:p.Lys1330Thr
NR_104109.1:n.1433A>C (ATP7A)
NR_104109.2:n.1396A>C (ATP7A)
ENST00000341514.10:c.4223A>C (ATP7A) ENSP00000345728.6:p.Lys1408Thr
ENST00000343533.10:c.4253A>C (ATP7A) ENSP00000343026.6:p.Lys1418Thr
ENST00000343533.9:c.3989A>C (ATP7A) ENSP00000343026.5:p.Lys1330Thr
ENST00000350425.5:c.*3396A>C (ATP7A) ENSP00000343678.5:n.*3396A>C
ENST00000644362.1:c.-19-64298A>C (PGK1) ENSP00000496140.1:n.-19-64298A>C
ENST00000682475.1:n.2640A>C (ATP7A)
ENST00000685033.1:c.1487A>C (ATP7A) ENSP00000509269.1:p.Lys496Thr
ENST00000685264.1:c.4223A>C (ATP7A) ENSP00000510136.1:p.Lys1408Thr
ENST00000686033.1:c.4028A>C (ATP7A) ENSP00000510693.1:p.Lys1343Thr
ENST00000686133.1:c.4223A>C (ATP7A) ENSP00000509233.1:p.Lys1408Thr
ENST00000686255.1:n.3254A>C (ATP7A)
ENST00000686543.1:c.3989A>C (ATP7A) ENSP00000509477.1:p.Lys1330Thr
ENST00000687086.1:c.4223A>C (ATP7A) ENSP00000509566.1:p.Lys1408Thr
ENST00000689083.1:n.1518A>C (ATP7A)
ENST00000689767.1:c.4316A>C (ATP7A) ENSP00000509406.1:p.Lys1439Thr
ENST00000692908.1:c.3989A>C (ATP7A) ENSP00000508627.1:p.Lys1330Thr