Canonical Allele Identifier: CA403091912

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7598541T>C (hg19) ; chr19:g.7533655T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7533655T>C , CM000681.2:g.7533655T>C	GRCh38
NC_000019.9:g.7598541T>C , CM000681.1:g.7598541T>C	GRCh37
NC_000019.8:g.7504541T>C	NCBI36
NG_013374.1:g.4504T>C
NG_015806.1:g.16046T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264079.11:c.1706+2T>C MANE Select	ENSP00000264079.5:n.1706+2T>C
ENST00000264079.10:c.1706+2T>C	ENSP00000264079.5:n.1706+2T>C
ENST00000394321.9:n.2021+2T>C
ENST00000599334.1:c.434+2T>C
ENST00000601870.1:c.59+2T>C
ENST00000602227.1:n.260+2T>C
NM_020533.2:c.1706+2T>C	NP_065394.1:n.1706+2T>C
NM_020533.3:c.1706+2T>C MANE Select	NP_065394.1:n.1706+2T>C