Canonical Allele Identifier: CA6619816

Gene: PMEL

Linked Data

• dbSNP Id: rs753104093
• ExAC: 12:56348092 G / C
• gnomAD v2: 12-56348092-G-C
• gnomAD v3: 12-55954308-G-C
• gnomAD v4: 12-55954308-G-C
• MyVariant Identifiers: chr12:g.56348092G>C (hg19) ; chr12:g.55954308G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55954308G>C , CM000674.2:g.55954308G>C	GRCh38
NC_000012.11:g.56348092G>C , CM000674.1:g.56348092G>C	GRCh37
NC_000012.10:g.54634359G>C	NCBI36
NG_028086.1:g.17405C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000548747.6:c.1892C>G MANE Select	ENSP00000448828.1:p.Pro631Arg
ENST00000449260.6:c.1913C>G	ENSP00000402758.2:p.Pro638Arg
ENST00000548493.5:c.1892C>G	ENSP00000447374.1:p.Pro631Arg
ENST00000548747.5:c.1892C>G	ENSP00000448828.1:p.Pro631Arg
ENST00000549564.1:n.471C>G
ENST00000550447.5:c.779C>G	ENSP00000448029.1:p.Pro260Arg
ENST00000550464.5:c.1634C>G	ENSP00000450036.1:p.Pro545Arg
ENST00000552882.5:c.1892C>G	ENSP00000449690.1:p.Pro631Arg
NM_001200053.1:c.1634C>G	NP_001186982.1:p.Pro545Arg
NM_001200054.1:c.1913C>G	NP_001186983.1:p.Pro638Arg
NM_006928.4:c.1892C>G	NP_008859.1:p.Pro631Arg
XM_006719569.1:c.1892C>G	XP_006719632.1:p.Pro631Arg
XM_011538685.1:c.1913C>G	XP_011536987.1:p.Pro638Arg
XM_011538686.1:c.1787C>G	XP_011536988.1:p.Pro596Arg
XM_011538687.1:c.1766C>G	XP_011536989.1:p.Pro589Arg
NM_001320121.1:c.1787C>G	NP_001307050.1:p.Pro596Arg
NM_001320122.1:c.1766C>G	NP_001307051.1:p.Pro589Arg
NM_001384361.1:c.1892C>G MANE Select	NP_001371290.1:p.Pro631Arg
NM_006928.5:c.1892C>G	NP_008859.1:p.Pro631Arg