Canonical Allele Identifier: CA2619240951
Gene: PMEL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55957100_55957101insAGCACACAGCTGCCTCCATCAGCCACCAAAGTAGGCAAGACTCACGGACAATGTCCAG , CM000674.2:g.55957100_55957101insAGCACACAGCTGCCTCCATCAGCCACCAAAGTAGGCAAGACTCACGGACAATGTCCAG GRCh38
NC_000012.11:g.56350884_56350885insAGCACACAGCTGCCTCCATCAGCCACCAAAGTAGGCAAGACTCACGGACAATGTCCAG , CM000674.1:g.56350884_56350885insAGCACACAGCTGCCTCCATCAGCCACCAAAGTAGGCAAGACTCACGGACAATGTCCAG GRCh37
NC_000012.10:g.54637151_54637152insAGCACACAGCTGCCTCCATCAGCCACCAAAGTAGGCAAGACTCACGGACAATGTCCAG NCBI36
NG_028086.1:g.14612_14613insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000548747.6:c.1202_1203insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT MANE Select ENSP00000448828.1:p.Pro402TrpfsTer13
ENST00000449260.6:c.1202_1203insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT ENSP00000402758.2:p.Pro402TrpfsTer13
ENST00000548493.5:c.1202_1203insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT ENSP00000447374.1:p.Pro402TrpfsTer13
ENST00000548747.5:c.1202_1203insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT ENSP00000448828.1:p.Pro402TrpfsTer13
ENST00000548803.5:c.671-42_671-41insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT ENSP00000447732.1:n.671-42_671-41insCTGGA...
ENST00000549404.5:c.780-42_780-41insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT
ENST00000549564.1:n.235+7_235+8insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT
ENST00000550447.5:c.359-1238_359-1237insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT ENSP00000448029.1:n.359-1238_359-1237insC...
ENST00000550464.5:c.944_945insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT ENSP00000450036.1:p.Pro316TrpfsTer13
ENST00000552882.5:c.1202_1203insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT ENSP00000449690.1:p.Pro402TrpfsTer13
NM_001200053.1:c.944_945insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT NP_001186982.1:p.Pro316TrpfsTer13
NM_001200054.1:c.1202_1203insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT NP_001186983.1:p.Pro402TrpfsTer13
NM_006928.4:c.1202_1203insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT NP_008859.1:p.Pro402TrpfsTer13
XM_006719569.1:c.1202_1203insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT XP_006719632.1:p.Pro402TrpfsTer13
XM_011538685.1:c.1202_1203insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT XP_011536987.1:p.Pro402TrpfsTer13
XM_011538686.1:c.1118-42_1118-41insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT XP_011536988.1:n.1118-42_1118-41insCTGGAC...
XM_011538687.1:c.1118-42_1118-41insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT XP_011536989.1:n.1118-42_1118-41insCTGGAC...
NM_001320121.1:c.1118-42_1118-41insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT NP_001307050.1:n.1118-42_1118-41insCTGGAC...
NM_001320122.1:c.1118-42_1118-41insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT NP_001307051.1:n.1118-42_1118-41insCTGGAC...
NM_001384361.1:c.1202_1203insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT MANE Select NP_001371290.1:p.Pro402TrpfsTer13
NM_006928.5:c.1202_1203insCTGGACATTGTCCGTGAGTCTTGCCTACTTTGGTGGCTGATGGAGGCAGCTGTGTGCT NP_008859.1:p.Pro402TrpfsTer13