Canonical Allele Identifier: CA480364902

Gene: PMEL

Linked Data

• MyVariant Identifiers: chr12:g.56351073A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55957289A>T , CM000674.2:g.55957289A>T	GRCh38
NC_000012.11:g.56351073A>T , CM000674.1:g.56351073A>T	GRCh37
NC_000012.10:g.54637340A>T	NCBI36
NG_028086.1:g.14424T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000548747.6:c.1014T>A MANE Select	ENSP00000448828.1:p.Gly338=
ENST00000449260.6:c.1014T>A	ENSP00000402758.2:p.Gly338=
ENST00000546543.5:c.867T>A	ENSP00000446662.1:p.Gly289=
ENST00000547137.5:c.852T>A	ENSP00000448849.1:p.Gly284=
ENST00000548493.5:c.1014T>A	ENSP00000447374.1:p.Gly338=
ENST00000548747.5:c.1014T>A	ENSP00000448828.1:p.Gly338=
ENST00000548803.5:c.567T>A	ENSP00000447732.1:p.Gly189=
ENST00000549404.5:c.676T>A
ENST00000549564.1:n.54T>A
ENST00000550447.5:c.358+1184T>A	ENSP00000448029.1:n.358+1184T>A
ENST00000550464.5:c.756T>A	ENSP00000450036.1:p.Gly252=
ENST00000552882.5:c.1014T>A	ENSP00000449690.1:p.Gly338=
ENST00000556802.1:n.750T>A
NM_001200053.1:c.756T>A	NP_001186982.1:p.Gly252=
NM_001200054.1:c.1014T>A	NP_001186983.1:p.Gly338=
NM_006928.4:c.1014T>A	NP_008859.1:p.Gly338=
XM_006719569.1:c.1014T>A	XP_006719632.1:p.Gly338=
XM_011538685.1:c.1014T>A	XP_011536987.1:p.Gly338=
XM_011538686.1:c.1014T>A	XP_011536988.1:p.Gly338=
XM_011538687.1:c.1014T>A	XP_011536989.1:p.Gly338=
NM_001320121.1:c.1014T>A	NP_001307050.1:p.Gly338=
NM_001320122.1:c.1014T>A	NP_001307051.1:p.Gly338=
NM_001384361.1:c.1014T>A MANE Select	NP_001371290.1:p.Gly338=
NM_006928.5:c.1014T>A	NP_008859.1:p.Gly338=