Canonical Allele Identifier: CA385214650

Gene: PMEL

Linked Data

• dbSNP Id: rs1592762444
• MyVariant Identifiers: chr12:g.56348039T>G (hg19) ; chr12:g.55954255T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55954255T>G , CM000674.2:g.55954255T>G	GRCh38
NC_000012.11:g.56348039T>G , CM000674.1:g.56348039T>G	GRCh37
NC_000012.10:g.54634306T>G	NCBI36
NG_028086.1:g.17458A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548747.6:c.1945A>C MANE Select	ENSP00000448828.1:p.Ile649Leu
ENST00000449260.6:c.1966A>C	ENSP00000402758.2:p.Ile656Leu
ENST00000548493.5:c.1945A>C	ENSP00000447374.1:p.Ile649Leu
ENST00000548747.5:c.1945A>C	ENSP00000448828.1:p.Ile649Leu
ENST00000550447.5:c.832A>C	ENSP00000448029.1:p.Ile278Leu
ENST00000550464.5:c.1687A>C	ENSP00000450036.1:p.Ile563Leu
ENST00000552882.5:c.1945A>C	ENSP00000449690.1:p.Ile649Leu
NM_001200053.1:c.1687A>C	NP_001186982.1:p.Ile563Leu
NM_001200054.1:c.1966A>C	NP_001186983.1:p.Ile656Leu
NM_006928.4:c.1945A>C	NP_008859.1:p.Ile649Leu
XM_006719569.1:c.1945A>C	XP_006719632.1:p.Ile649Leu
XM_011538685.1:c.1966A>C	XP_011536987.1:p.Ile656Leu
XM_011538686.1:c.1840A>C	XP_011536988.1:p.Ile614Leu
XM_011538687.1:c.1819A>C	XP_011536989.1:p.Ile607Leu
NM_001320121.1:c.1840A>C	NP_001307050.1:p.Ile614Leu
NM_001320122.1:c.1819A>C	NP_001307051.1:p.Ile607Leu
NM_001384361.1:c.1945A>C MANE Select	NP_001371290.1:p.Ile649Leu
NM_006928.5:c.1945A>C	NP_008859.1:p.Ile649Leu