Canonical Allele Identifier: CA385214822

Gene: PMEL

Linked Data

• MyVariant Identifiers: chr12:g.56348118C>A (hg19) ; chr12:g.55954334C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55954334C>A , CM000674.2:g.55954334C>A	GRCh38
NC_000012.11:g.56348118C>A , CM000674.1:g.56348118C>A	GRCh37
NC_000012.10:g.54634385C>A	NCBI36
NG_028086.1:g.17379G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548747.6:c.1866G>T MANE Select	ENSP00000448828.1:p.Lys622Asn
ENST00000449260.6:c.1887G>T	ENSP00000402758.2:p.Lys629Asn
ENST00000548493.5:c.1866G>T	ENSP00000447374.1:p.Lys622Asn
ENST00000548747.5:c.1866G>T	ENSP00000448828.1:p.Lys622Asn
ENST00000549564.1:n.445G>T
ENST00000550447.5:c.753G>T	ENSP00000448029.1:p.Lys251Asn
ENST00000550464.5:c.1608G>T	ENSP00000450036.1:p.Lys536Asn
ENST00000552882.5:c.1866G>T	ENSP00000449690.1:p.Lys622Asn
NM_001200053.1:c.1608G>T	NP_001186982.1:p.Lys536Asn
NM_001200054.1:c.1887G>T	NP_001186983.1:p.Lys629Asn
NM_006928.4:c.1866G>T	NP_008859.1:p.Lys622Asn
XM_006719569.1:c.1866G>T	XP_006719632.1:p.Lys622Asn
XM_011538685.1:c.1887G>T	XP_011536987.1:p.Lys629Asn
XM_011538686.1:c.1761G>T	XP_011536988.1:p.Lys587Asn
XM_011538687.1:c.1740G>T	XP_011536989.1:p.Lys580Asn
NM_001320121.1:c.1761G>T	NP_001307050.1:p.Lys587Asn
NM_001320122.1:c.1740G>T	NP_001307051.1:p.Lys580Asn
NM_001384361.1:c.1866G>T MANE Select	NP_001371290.1:p.Lys622Asn
NM_006928.5:c.1866G>T	NP_008859.1:p.Lys622Asn