Canonical Allele Identifier: CA385214645

Gene: PMEL

Linked Data

• MyVariant Identifiers: chr12:g.56348038A>C (hg19) ; chr12:g.55954254A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55954254A>C , CM000674.2:g.55954254A>C	GRCh38
NC_000012.11:g.56348038A>C , CM000674.1:g.56348038A>C	GRCh37
NC_000012.10:g.54634305A>C	NCBI36
NG_028086.1:g.17459T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548747.6:c.1946T>G MANE Select	ENSP00000448828.1:p.Ile649Ser
ENST00000449260.6:c.1967T>G	ENSP00000402758.2:p.Ile656Ser
ENST00000548493.5:c.1946T>G	ENSP00000447374.1:p.Ile649Ser
ENST00000548747.5:c.1946T>G	ENSP00000448828.1:p.Ile649Ser
ENST00000550447.5:c.833T>G	ENSP00000448029.1:p.Ile278Ser
ENST00000550464.5:c.1688T>G	ENSP00000450036.1:p.Ile563Ser
ENST00000552882.5:c.1946T>G	ENSP00000449690.1:p.Ile649Ser
NM_001200053.1:c.1688T>G	NP_001186982.1:p.Ile563Ser
NM_001200054.1:c.1967T>G	NP_001186983.1:p.Ile656Ser
NM_006928.4:c.1946T>G	NP_008859.1:p.Ile649Ser
XM_006719569.1:c.1946T>G	XP_006719632.1:p.Ile649Ser
XM_011538685.1:c.1967T>G	XP_011536987.1:p.Ile656Ser
XM_011538686.1:c.1841T>G	XP_011536988.1:p.Ile614Ser
XM_011538687.1:c.1820T>G	XP_011536989.1:p.Ile607Ser
NM_001320121.1:c.1841T>G	NP_001307050.1:p.Ile614Ser
NM_001320122.1:c.1820T>G	NP_001307051.1:p.Ile607Ser
NM_001384361.1:c.1946T>G MANE Select	NP_001371290.1:p.Ile649Ser
NM_006928.5:c.1946T>G	NP_008859.1:p.Ile649Ser