Canonical Allele Identifier: CA385216793

Gene: PMEL

Linked Data

• MyVariant Identifiers: chr12:g.56350835C>T (hg19) ; chr12:g.55957051C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55957051C>T , CM000674.2:g.55957051C>T	GRCh38
NC_000012.11:g.56350835C>T , CM000674.1:g.56350835C>T	GRCh37
NC_000012.10:g.54637102C>T	NCBI36
NG_028086.1:g.14662G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548747.6:c.1252G>A MANE Select	ENSP00000448828.1:p.Val418Ile
ENST00000449260.6:c.1252G>A	ENSP00000402758.2:p.Val418Ile
ENST00000548493.5:c.1252G>A	ENSP00000447374.1:p.Val418Ile
ENST00000548747.5:c.1252G>A	ENSP00000448828.1:p.Val418Ile
ENST00000548803.5:c.679G>A	ENSP00000447732.1:p.Val227Ile
ENST00000549404.5:c.788G>A
ENST00000549564.1:n.235+57G>A
ENST00000550447.5:c.359-1188G>A	ENSP00000448029.1:n.359-1188G>A
ENST00000550464.5:c.994G>A	ENSP00000450036.1:p.Val332Ile
ENST00000552882.5:c.1252G>A	ENSP00000449690.1:p.Val418Ile
NM_001200053.1:c.994G>A	NP_001186982.1:p.Val332Ile
NM_001200054.1:c.1252G>A	NP_001186983.1:p.Val418Ile
NM_006928.4:c.1252G>A	NP_008859.1:p.Val418Ile
XM_006719569.1:c.1252G>A	XP_006719632.1:p.Val418Ile
XM_011538685.1:c.1252G>A	XP_011536987.1:p.Val418Ile
XM_011538686.1:c.1126G>A	XP_011536988.1:p.Val376Ile
XM_011538687.1:c.1126G>A	XP_011536989.1:p.Val376Ile
NM_001320121.1:c.1126G>A	NP_001307050.1:p.Val376Ile
NM_001320122.1:c.1126G>A	NP_001307051.1:p.Val376Ile
NM_001384361.1:c.1252G>A MANE Select	NP_001371290.1:p.Val418Ile
NM_006928.5:c.1252G>A	NP_008859.1:p.Val418Ile