Canonical Allele Identifier: CA2038181154
Gene: PMEL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55957098G= , CM000674.2:g.55957098G= GRCh38
NC_000012.11:g.56350882G= , CM000674.1:g.56350882G= GRCh37
NC_000012.10:g.54637149G= NCBI36
NG_028086.1:g.14615C=

Transcript Alleles

HGVS Amino-acid change
ENST00000548747.6:c.1205C= MANE Select ENSP00000448828.1:p.Pro402=
ENST00000449260.6:c.1205C= ENSP00000402758.2:p.Pro402=
ENST00000548493.5:c.1205C= ENSP00000447374.1:p.Pro402=
ENST00000548747.5:c.1205C= ENSP00000448828.1:p.Pro402=
ENST00000548803.5:c.671-39C= ENSP00000447732.1:n.671-39C=
ENST00000549404.5:c.780-39C=
ENST00000549564.1:n.235+10C=
ENST00000550447.5:c.359-1235C= ENSP00000448029.1:n.359-1235C=
ENST00000550464.5:c.947C= ENSP00000450036.1:p.Pro316=
ENST00000552882.5:c.1205C= ENSP00000449690.1:p.Pro402=
NM_001200053.1:c.947C= NP_001186982.1:p.Pro316=
NM_001200054.1:c.1205C= NP_001186983.1:p.Pro402=
NM_006928.4:c.1205C= NP_008859.1:p.Pro402=
XM_006719569.1:c.1205C= XP_006719632.1:p.Pro402=
XM_011538685.1:c.1205C= XP_011536987.1:p.Pro402=
XM_011538686.1:c.1118-39C= XP_011536988.1:n.1118-39C=
XM_011538687.1:c.1118-39C= XP_011536989.1:n.1118-39C=
NM_001320121.1:c.1118-39C= NP_001307050.1:n.1118-39C=
NM_001320122.1:c.1118-39C= NP_001307051.1:n.1118-39C=
NM_001384361.1:c.1205C= MANE Select NP_001371290.1:p.Pro402=
NM_006928.5:c.1205C= NP_008859.1:p.Pro402=