Canonical Allele Identifier: CA505233439

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7598675G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7533789G>C , CM000681.2:g.7533789G>C	GRCh38
NC_000019.9:g.7598675G>C , CM000681.1:g.7598675G>C	GRCh37
NC_000019.8:g.7504675G>C	NCBI36
NG_013374.1:g.4638G>C
NG_015806.1:g.16180G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.1737G>C MANE Select	ENSP00000264079.5:p.Val579=
ENST00000264079.10:c.1737G>C	ENSP00000264079.5:p.Val579=
ENST00000394321.9:n.2052G>C
ENST00000599334.1:c.465G>C
ENST00000601870.1:c.90G>C
ENST00000602227.1:n.291G>C
NM_020533.2:c.1737G>C	NP_065394.1:p.Val579=
NM_020533.3:c.1737G>C MANE Select	NP_065394.1:p.Val579=