Canonical Allele Identifier: CA2038177419
Gene: PMEL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55954198C= , CM000674.2:g.55954198C= GRCh38
NC_000012.11:g.56347982C= , CM000674.1:g.56347982C= GRCh37
NC_000012.10:g.54634249C= NCBI36
NG_028086.1:g.17515G=

Transcript Alleles

HGVS Amino-acid change
ENST00000548747.6:c.*16G= MANE Select ENSP00000448828.1:n.*16G=
ENST00000449260.6:c.*16G= ENSP00000402758.2:n.*16G=
ENST00000548493.5:c.*16G= ENSP00000447374.1:n.*16G=
ENST00000548747.5:c.*16G= ENSP00000448828.1:n.*16G=
ENST00000550464.5:c.*16G= ENSP00000450036.1:n.*16G=
ENST00000552882.5:c.*16G= ENSP00000449690.1:n.*16G=
NM_001200053.1:c.*16G= NP_001186982.1:n.*16G=
NM_001200054.1:c.*16G= NP_001186983.1:n.*16G=
NM_006928.4:c.*16G= NP_008859.1:n.*16G=
XM_006719569.1:c.*16G= XP_006719632.1:n.*16G=
XM_011538685.1:c.*16G= XP_011536987.1:n.*16G=
XM_011538686.1:c.*16G= XP_011536988.1:n.*16G=
XM_011538687.1:c.*16G= XP_011536989.1:n.*16G=
NM_001320121.1:c.*16G= NP_001307050.1:n.*16G=
NM_001320122.1:c.*16G= NP_001307051.1:n.*16G=
NM_001384361.1:c.*16G= MANE Select NP_001371290.1:n.*16G=
NM_006928.5:c.*16G= NP_008859.1:n.*16G=