Canonical Allele Identifier: CA2038181236

Gene: PMEL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55957148C= , CM000674.2:g.55957148C=	GRCh38
NC_000012.11:g.56350932C= , CM000674.1:g.56350932C=	GRCh37
NC_000012.10:g.54637199C=	NCBI36
NG_028086.1:g.14565G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000548747.6:c.1155G= MANE Select	ENSP00000448828.1:p.Met385=
ENST00000449260.6:c.1155G=	ENSP00000402758.2:p.Met385=
ENST00000547137.5:c.993G=	ENSP00000448849.1:p.Met331=
ENST00000548493.5:c.1155G=	ENSP00000447374.1:p.Met385=
ENST00000548747.5:c.1155G=	ENSP00000448828.1:p.Met385=
ENST00000548803.5:c.670+38G=	ENSP00000447732.1:n.670+38G=
ENST00000549404.5:c.779+38G=
ENST00000549564.1:n.195G=
ENST00000550447.5:c.359-1285G=	ENSP00000448029.1:n.359-1285G=
ENST00000550464.5:c.897G=	ENSP00000450036.1:p.Met299=
ENST00000552882.5:c.1155G=	ENSP00000449690.1:p.Met385=
NM_001200053.1:c.897G=	NP_001186982.1:p.Met299=
NM_001200054.1:c.1155G=	NP_001186983.1:p.Met385=
NM_006928.4:c.1155G=	NP_008859.1:p.Met385=
XM_006719569.1:c.1155G=	XP_006719632.1:p.Met385=
XM_011538685.1:c.1155G=	XP_011536987.1:p.Met385=
XM_011538686.1:c.1117+38G=	XP_011536988.1:n.1117+38G=
XM_011538687.1:c.1117+38G=	XP_011536989.1:n.1117+38G=
NM_001320121.1:c.1117+38G=	NP_001307050.1:n.1117+38G=
NM_001320122.1:c.1117+38G=	NP_001307051.1:n.1117+38G=
NM_001384361.1:c.1155G= MANE Select	NP_001371290.1:p.Met385=
NM_006928.5:c.1155G=	NP_008859.1:p.Met385=