Canonical Allele Identifier: CA505231724

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7594490A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7529604A>C , CM000681.2:g.7529604A>C	GRCh38
NC_000019.9:g.7594490A>C , CM000681.1:g.7594490A>C	GRCh37
NC_000019.8:g.7500490A>C	NCBI36
NG_013374.1:g.453A>C
NG_015806.1:g.11995A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.1251A>C MANE Select	ENSP00000264079.5:p.Thr417=
ENST00000264079.10:c.1251A>C	ENSP00000264079.5:p.Thr417=
ENST00000394321.9:n.1566A>C
ENST00000594692.1:n.247A>C
ENST00000595860.5:n.434A>C
ENST00000599334.1:c.128A>C
NM_020533.2:c.1251A>C	NP_065394.1:p.Thr417=
NM_020533.3:c.1251A>C MANE Select	NP_065394.1:p.Thr417=