Canonical Allele Identifier: CA2038177639

Gene: PMEL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55954321C= , CM000674.2:g.55954321C=	GRCh38
NC_000012.11:g.56348105C= , CM000674.1:g.56348105C=	GRCh37
NC_000012.10:g.54634372C=	NCBI36
NG_028086.1:g.17392G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548747.6:c.1879G= MANE Select	ENSP00000448828.1:p.Val627=
ENST00000449260.6:c.1900G=	ENSP00000402758.2:p.Val634=
ENST00000548493.5:c.1879G=	ENSP00000447374.1:p.Val627=
ENST00000548747.5:c.1879G=	ENSP00000448828.1:p.Val627=
ENST00000549564.1:n.458G=
ENST00000550447.5:c.766G=	ENSP00000448029.1:p.Val256=
ENST00000550464.5:c.1621G=	ENSP00000450036.1:p.Val541=
ENST00000552882.5:c.1879G=	ENSP00000449690.1:p.Val627=
NM_001200053.1:c.1621G=	NP_001186982.1:p.Val541=
NM_001200054.1:c.1900G=	NP_001186983.1:p.Val634=
NM_006928.4:c.1879G=	NP_008859.1:p.Val627=
XM_006719569.1:c.1879G=	XP_006719632.1:p.Val627=
XM_011538685.1:c.1900G=	XP_011536987.1:p.Val634=
XM_011538686.1:c.1774G=	XP_011536988.1:p.Val592=
XM_011538687.1:c.1753G=	XP_011536989.1:p.Val585=
NM_001320121.1:c.1774G=	NP_001307050.1:p.Val592=
NM_001320122.1:c.1753G=	NP_001307051.1:p.Val585=
NM_001384361.1:c.1879G= MANE Select	NP_001371290.1:p.Val627=
NM_006928.5:c.1879G=	NP_008859.1:p.Val627=