Canonical Allele Identifier: CA403088066

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7594573T>C (hg19) ; chr19:g.7529687T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7529687T>C , CM000681.2:g.7529687T>C	GRCh38
NC_000019.9:g.7594573T>C , CM000681.1:g.7594573T>C	GRCh37
NC_000019.8:g.7500573T>C	NCBI36
NG_013374.1:g.536T>C
NG_015806.1:g.12078T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.1334T>C MANE Select	ENSP00000264079.5:p.Ile445Thr
ENST00000264079.10:c.1334T>C	ENSP00000264079.5:p.Ile445Thr
ENST00000394321.9:n.1649T>C
ENST00000594692.1:n.330T>C
ENST00000595860.5:n.517T>C
ENST00000599334.1:c.211T>C
NM_020533.2:c.1334T>C	NP_065394.1:p.Ile445Thr
NM_020533.3:c.1334T>C MANE Select	NP_065394.1:p.Ile445Thr