Canonical Allele Identifier: CA2619238163

Gene: PMEL

Linked Data

• gnomAD v4: 12-55954447-T-TCTCTACAAAATACATTTAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55954447_55954448insCTCTACAAAATACATTTAAAAAAA , CM000674.2:g.55954447_55954448insCTCTACAAAATACATTTAAAAAAA	GRCh38
NC_000012.11:g.56348231_56348232insCTCTACAAAATACATTTAAAAAAA , CM000674.1:g.56348231_56348232insCTCTACAAAATACATTTAAAAAAA	GRCh37
NC_000012.10:g.54634498_54634499insCTCTACAAAATACATTTAAAAAAA	NCBI36
NG_028086.1:g.17265_17266insTTTTTTTAAATGTATTTTGTAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548747.6:c.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG MANE Select	ENSP00000448828.1:n.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGA...
ENST00000449260.6:c.1872-99_1872-98insTTTTTTTAAATGTATTTTGTAGAG	ENSP00000402758.2:n.1872-99_1872-98insTTTTTTTAAATGTATTTTGTAGA...
ENST00000548493.5:c.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG	ENSP00000447374.1:n.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGA...
ENST00000548747.5:c.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG	ENSP00000448828.1:n.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGA...
ENST00000549564.1:n.430-99_430-98insTTTTTTTAAATGTATTTTGTAGAG
ENST00000550447.5:c.738-99_738-98insTTTTTTTAAATGTATTTTGTAGAG	ENSP00000448029.1:n.738-99_738-98insTTTTTTTAAATGTATTTTGTAGAG
ENST00000550464.5:c.1593-99_1593-98insTTTTTTTAAATGTATTTTGTAGAG	ENSP00000450036.1:n.1593-99_1593-98insTTTTTTTAAATGTATTTTGTAGA...
ENST00000552882.5:c.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG	ENSP00000449690.1:n.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGA...
NM_001200053.1:c.1593-99_1593-98insTTTTTTTAAATGTATTTTGTAGAG	NP_001186982.1:n.1593-99_1593-98insTTTTTTTAAATGTATTTTGTAGAG
NM_001200054.1:c.1872-99_1872-98insTTTTTTTAAATGTATTTTGTAGAG	NP_001186983.1:n.1872-99_1872-98insTTTTTTTAAATGTATTTTGTAGAG
NM_006928.4:c.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG	NP_008859.1:n.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG
XM_006719569.1:c.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG	XP_006719632.1:n.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG
XM_011538685.1:c.1872-99_1872-98insTTTTTTTAAATGTATTTTGTAGAG	XP_011536987.1:n.1872-99_1872-98insTTTTTTTAAATGTATTTTGTAGAG
XM_011538686.1:c.1746-99_1746-98insTTTTTTTAAATGTATTTTGTAGAG	XP_011536988.1:n.1746-99_1746-98insTTTTTTTAAATGTATTTTGTAGAG
XM_011538687.1:c.1725-99_1725-98insTTTTTTTAAATGTATTTTGTAGAG	XP_011536989.1:n.1725-99_1725-98insTTTTTTTAAATGTATTTTGTAGAG
NM_001320121.1:c.1746-99_1746-98insTTTTTTTAAATGTATTTTGTAGAG	NP_001307050.1:n.1746-99_1746-98insTTTTTTTAAATGTATTTTGTAGAG
NM_001320122.1:c.1725-99_1725-98insTTTTTTTAAATGTATTTTGTAGAG	NP_001307051.1:n.1725-99_1725-98insTTTTTTTAAATGTATTTTGTAGAG
NM_001384361.1:c.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG MANE Select	NP_001371290.1:n.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG
NM_006928.5:c.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG	NP_008859.1:n.1851-99_1851-98insTTTTTTTAAATGTATTTTGTAGAG