Canonical Allele Identifier: CA2038181040

Gene: PMEL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55957047G= , CM000674.2:g.55957047G=	GRCh38
NC_000012.11:g.56350831G= , CM000674.1:g.56350831G=	GRCh37
NC_000012.10:g.54637098G=	NCBI36
NG_028086.1:g.14666C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548747.6:c.1256C= MANE Select	ENSP00000448828.1:p.Thr419=
ENST00000449260.6:c.1256C=	ENSP00000402758.2:p.Thr419=
ENST00000548493.5:c.1256C=	ENSP00000447374.1:p.Thr419=
ENST00000548747.5:c.1256C=	ENSP00000448828.1:p.Thr419=
ENST00000548803.5:c.683C=	ENSP00000447732.1:p.Thr228=
ENST00000549404.5:c.792C=
ENST00000549564.1:n.235+61C=
ENST00000550447.5:c.359-1184C=	ENSP00000448029.1:n.359-1184C=
ENST00000550464.5:c.998C=	ENSP00000450036.1:p.Thr333=
ENST00000552882.5:c.1256C=	ENSP00000449690.1:p.Thr419=
NM_001200053.1:c.998C=	NP_001186982.1:p.Thr333=
NM_001200054.1:c.1256C=	NP_001186983.1:p.Thr419=
NM_006928.4:c.1256C=	NP_008859.1:p.Thr419=
XM_006719569.1:c.1256C=	XP_006719632.1:p.Thr419=
XM_011538685.1:c.1256C=	XP_011536987.1:p.Thr419=
XM_011538686.1:c.1130C=	XP_011536988.1:p.Thr377=
XM_011538687.1:c.1130C=	XP_011536989.1:p.Thr377=
NM_001320121.1:c.1130C=	NP_001307050.1:p.Thr377=
NM_001320122.1:c.1130C=	NP_001307051.1:p.Thr377=
NM_001384361.1:c.1256C= MANE Select	NP_001371290.1:p.Thr419=
NM_006928.5:c.1256C=	NP_008859.1:p.Thr419=