Canonical Allele Identifier: CA385214573

Gene: PMEL

Linked Data

• MyVariant Identifiers: chr12:g.56348004C>G (hg19) ; chr12:g.55954220C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55954220C>G , CM000674.2:g.55954220C>G	GRCh38
NC_000012.11:g.56348004C>G , CM000674.1:g.56348004C>G	GRCh37
NC_000012.10:g.54634271C>G	NCBI36
NG_028086.1:g.17493G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548747.6:c.1980G>C MANE Select	ENSP00000448828.1:p.Gln660His
ENST00000449260.6:c.2001G>C	ENSP00000402758.2:p.Gln667His
ENST00000548493.5:c.1980G>C	ENSP00000447374.1:p.Gln660His
ENST00000548747.5:c.1980G>C	ENSP00000448828.1:p.Gln660His
ENST00000550447.5:c.867G>C	ENSP00000448029.1:p.Gln289His
ENST00000550464.5:c.1722G>C	ENSP00000450036.1:p.Gln574His
ENST00000552882.5:c.1980G>C	ENSP00000449690.1:p.Gln660His
NM_001200053.1:c.1722G>C	NP_001186982.1:p.Gln574His
NM_001200054.1:c.2001G>C	NP_001186983.1:p.Gln667His
NM_006928.4:c.1980G>C	NP_008859.1:p.Gln660His
XM_006719569.1:c.1980G>C	XP_006719632.1:p.Gln660His
XM_011538685.1:c.2001G>C	XP_011536987.1:p.Gln667His
XM_011538686.1:c.1875G>C	XP_011536988.1:p.Gln625His
XM_011538687.1:c.1854G>C	XP_011536989.1:p.Gln618His
NM_001320121.1:c.1875G>C	NP_001307050.1:p.Gln625His
NM_001320122.1:c.1854G>C	NP_001307051.1:p.Gln618His
NM_001384361.1:c.1980G>C MANE Select	NP_001371290.1:p.Gln660His
NM_006928.5:c.1980G>C	NP_008859.1:p.Gln660His