Canonical Allele Identifier: CA947964346
Gene: PMEL HGNC NCBI

Linked Data

dbSNP Id: rs1888748715

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55954355dup , CM000674.2:g.55954355dup GRCh38
NC_000012.11:g.56348139dup , CM000674.1:g.56348139dup GRCh37
NC_000012.10:g.54634406dup NCBI36
NG_028086.1:g.17358dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000548747.6:c.1851-6dup MANE Select ENSP00000448828.1:n.1851-6dup
ENST00000449260.6:c.1872-6dup ENSP00000402758.2:n.1872-6dup
ENST00000548493.5:c.1851-6dup ENSP00000447374.1:n.1851-6dup
ENST00000548747.5:c.1851-6dup ENSP00000448828.1:n.1851-6dup
ENST00000549564.1:n.430-6dup
ENST00000550447.5:c.738-6dup ENSP00000448029.1:n.738-6dup
ENST00000550464.5:c.1593-6dup ENSP00000450036.1:n.1593-6dup
ENST00000552882.5:c.1851-6dup ENSP00000449690.1:n.1851-6dup
NM_001200053.1:c.1593-6dup NP_001186982.1:n.1593-6dup
NM_001200054.1:c.1872-6dup NP_001186983.1:n.1872-6dup
NM_006928.4:c.1851-6dup NP_008859.1:n.1851-6dup
XM_006719569.1:c.1851-6dup XP_006719632.1:n.1851-6dup
XM_011538685.1:c.1872-6dup XP_011536987.1:n.1872-6dup
XM_011538686.1:c.1746-6dup XP_011536988.1:n.1746-6dup
XM_011538687.1:c.1725-6dup XP_011536989.1:n.1725-6dup
NM_001320121.1:c.1746-6dup NP_001307050.1:n.1746-6dup
NM_001320122.1:c.1725-6dup NP_001307051.1:n.1725-6dup
NM_001384361.1:c.1851-6dup MANE Select NP_001371290.1:n.1851-6dup
NM_006928.5:c.1851-6dup NP_008859.1:n.1851-6dup