Canonical Allele Identifier: CA403087058

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7594076C>A (hg19) ; chr19:g.7529190C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7529190C>A , CM000681.2:g.7529190C>A	GRCh38
NC_000019.9:g.7594076C>A , CM000681.1:g.7594076C>A	GRCh37
NC_000019.8:g.7500076C>A	NCBI36
NG_013374.1:g.39C>A
NG_015806.1:g.11581C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.1224C>A MANE Select	ENSP00000264079.5:p.Phe408Leu
ENST00000264079.10:c.1224C>A	ENSP00000264079.5:p.Phe408Leu
ENST00000394321.9:n.1539C>A
ENST00000594692.1:n.220C>A
ENST00000595860.5:n.407C>A
ENST00000599334.1:c.101C>A
NM_020533.2:c.1224C>A	NP_065394.1:p.Phe408Leu
NM_020533.3:c.1224C>A MANE Select	NP_065394.1:p.Phe408Leu