Canonical Allele Identifier: CA403089389

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7595231G>T (hg19) ; chr19:g.7530345G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7530345G>T , CM000681.2:g.7530345G>T	GRCh38
NC_000019.9:g.7595231G>T , CM000681.1:g.7595231G>T	GRCh37
NC_000019.8:g.7501231G>T	NCBI36
NG_013374.1:g.1194G>T
NG_015806.1:g.12736G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.1419G>T MANE Select	ENSP00000264079.5:p.Met473Ile
ENST00000264079.10:c.1419G>T	ENSP00000264079.5:p.Met473Ile
ENST00000394321.9:n.1734G>T
ENST00000594692.1:n.415G>T
ENST00000595860.5:n.602G>T
ENST00000599334.1:c.237-90G>T
NM_020533.2:c.1419G>T	NP_065394.1:p.Met473Ile
NM_020533.3:c.1419G>T MANE Select	NP_065394.1:p.Met473Ile