Canonical Allele Identifier: CA2038177841

Gene: PMEL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55954509G= , CM000674.2:g.55954509G=	GRCh38
NC_000012.11:g.56348293G= , CM000674.1:g.56348293G=	GRCh37
NC_000012.10:g.54634560G=	NCBI36
NG_028086.1:g.17204C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548747.6:c.1851-160C= MANE Select	ENSP00000448828.1:n.1851-160C=
ENST00000449260.6:c.1872-160C=	ENSP00000402758.2:n.1872-160C=
ENST00000548493.5:c.1851-160C=	ENSP00000447374.1:n.1851-160C=
ENST00000548747.5:c.1851-160C=	ENSP00000448828.1:n.1851-160C=
ENST00000549564.1:n.430-160C=
ENST00000550447.5:c.738-160C=	ENSP00000448029.1:n.738-160C=
ENST00000550464.5:c.1593-160C=	ENSP00000450036.1:n.1593-160C=
ENST00000552882.5:c.1851-160C=	ENSP00000449690.1:n.1851-160C=
NM_001200053.1:c.1593-160C=	NP_001186982.1:n.1593-160C=
NM_001200054.1:c.1872-160C=	NP_001186983.1:n.1872-160C=
NM_006928.4:c.1851-160C=	NP_008859.1:n.1851-160C=
XM_006719569.1:c.1851-160C=	XP_006719632.1:n.1851-160C=
XM_011538685.1:c.1872-160C=	XP_011536987.1:n.1872-160C=
XM_011538686.1:c.1746-160C=	XP_011536988.1:n.1746-160C=
XM_011538687.1:c.1725-160C=	XP_011536989.1:n.1725-160C=
NM_001320121.1:c.1746-160C=	NP_001307050.1:n.1746-160C=
NM_001320122.1:c.1725-160C=	NP_001307051.1:n.1725-160C=
NM_001384361.1:c.1851-160C= MANE Select	NP_001371290.1:n.1851-160C=
NM_006928.5:c.1851-160C=	NP_008859.1:n.1851-160C=