Canonical Allele Identifier: CA480178315

Gene: PMEL

Linked Data

• MyVariant Identifiers: chr12:g.56348040G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55954256G>A , CM000674.2:g.55954256G>A	GRCh38
NC_000012.11:g.56348040G>A , CM000674.1:g.56348040G>A	GRCh37
NC_000012.10:g.54634307G>A	NCBI36
NG_028086.1:g.17457C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548747.6:c.1944C>T MANE Select	ENSP00000448828.1:p.Pro648=
ENST00000449260.6:c.1965C>T	ENSP00000402758.2:p.Pro655=
ENST00000548493.5:c.1944C>T	ENSP00000447374.1:p.Pro648=
ENST00000548747.5:c.1944C>T	ENSP00000448828.1:p.Pro648=
ENST00000550447.5:c.831C>T	ENSP00000448029.1:p.Pro277=
ENST00000550464.5:c.1686C>T	ENSP00000450036.1:p.Pro562=
ENST00000552882.5:c.1944C>T	ENSP00000449690.1:p.Pro648=
NM_001200053.1:c.1686C>T	NP_001186982.1:p.Pro562=
NM_001200054.1:c.1965C>T	NP_001186983.1:p.Pro655=
NM_006928.4:c.1944C>T	NP_008859.1:p.Pro648=
XM_006719569.1:c.1944C>T	XP_006719632.1:p.Pro648=
XM_011538685.1:c.1965C>T	XP_011536987.1:p.Pro655=
XM_011538686.1:c.1839C>T	XP_011536988.1:p.Pro613=
XM_011538687.1:c.1818C>T	XP_011536989.1:p.Pro606=
NM_001320121.1:c.1839C>T	NP_001307050.1:p.Pro613=
NM_001320122.1:c.1818C>T	NP_001307051.1:p.Pro606=
NM_001384361.1:c.1944C>T MANE Select	NP_001371290.1:p.Pro648=
NM_006928.5:c.1944C>T	NP_008859.1:p.Pro648=