Canonical Allele Identifier: CA2038181178

Gene: PMEL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55957108C= , CM000674.2:g.55957108C=	GRCh38
NC_000012.11:g.56350892C= , CM000674.1:g.56350892C=	GRCh37
NC_000012.10:g.54637159C=	NCBI36
NG_028086.1:g.14605G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548747.6:c.1195G= MANE Select	ENSP00000448828.1:p.Gly399=
ENST00000449260.6:c.1195G=	ENSP00000402758.2:p.Gly399=
ENST00000548493.5:c.1195G=	ENSP00000447374.1:p.Gly399=
ENST00000548747.5:c.1195G=	ENSP00000448828.1:p.Gly399=
ENST00000548803.5:c.671-49G=	ENSP00000447732.1:n.671-49G=
ENST00000549404.5:c.780-49G=
ENST00000549564.1:n.235G=
ENST00000550447.5:c.359-1245G=	ENSP00000448029.1:n.359-1245G=
ENST00000550464.5:c.937G=	ENSP00000450036.1:p.Gly313=
ENST00000552882.5:c.1195G=	ENSP00000449690.1:p.Gly399=
NM_001200053.1:c.937G=	NP_001186982.1:p.Gly313=
NM_001200054.1:c.1195G=	NP_001186983.1:p.Gly399=
NM_006928.4:c.1195G=	NP_008859.1:p.Gly399=
XM_006719569.1:c.1195G=	XP_006719632.1:p.Gly399=
XM_011538685.1:c.1195G=	XP_011536987.1:p.Gly399=
XM_011538686.1:c.1118-49G=	XP_011536988.1:n.1118-49G=
XM_011538687.1:c.1118-49G=	XP_011536989.1:n.1118-49G=
NM_001320121.1:c.1118-49G=	NP_001307050.1:n.1118-49G=
NM_001320122.1:c.1118-49G=	NP_001307051.1:n.1118-49G=
NM_001384361.1:c.1195G= MANE Select	NP_001371290.1:p.Gly399=
NM_006928.5:c.1195G=	NP_008859.1:p.Gly399=