Canonical Allele Identifier: CA2619237780

Gene: PMEL

Linked Data

• gnomAD v4: 12-55954197-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55954197G>A , CM000674.2:g.55954197G>A	GRCh38
NC_000012.11:g.56347981G>A , CM000674.1:g.56347981G>A	GRCh37
NC_000012.10:g.54634248G>A	NCBI36
NG_028086.1:g.17516C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000548747.6:c.*17C>T MANE Select	ENSP00000448828.1:n.*17C>T
ENST00000449260.6:c.*17C>T	ENSP00000402758.2:n.*17C>T
ENST00000548493.5:c.*17C>T	ENSP00000447374.1:n.*17C>T
ENST00000548747.5:c.*17C>T	ENSP00000448828.1:n.*17C>T
ENST00000550464.5:c.*17C>T	ENSP00000450036.1:n.*17C>T
ENST00000552882.5:c.*17C>T	ENSP00000449690.1:n.*17C>T
NM_001200053.1:c.*17C>T	NP_001186982.1:n.*17C>T
NM_001200054.1:c.*17C>T	NP_001186983.1:n.*17C>T
NM_006928.4:c.*17C>T	NP_008859.1:n.*17C>T
XM_006719569.1:c.*17C>T	XP_006719632.1:n.*17C>T
XM_011538685.1:c.*17C>T	XP_011536987.1:n.*17C>T
XM_011538686.1:c.*17C>T	XP_011536988.1:n.*17C>T
XM_011538687.1:c.*17C>T	XP_011536989.1:n.*17C>T
NM_001320121.1:c.*17C>T	NP_001307050.1:n.*17C>T
NM_001320122.1:c.*17C>T	NP_001307051.1:n.*17C>T
NM_001384361.1:c.*17C>T MANE Select	NP_001371290.1:n.*17C>T
NM_006928.5:c.*17C>T	NP_008859.1:n.*17C>T