Canonical Allele Identifier: CA304853685

Gene: MCOLN1

Linked Data

• dbSNP Id: rs78838274
• MyVariant Identifiers: chr19:g.7592764C>G (hg19) ; chr19:g.7527878C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7527878C>G , CM000681.2:g.7527878C>G	GRCh38
NC_000019.9:g.7592764C>G , CM000681.1:g.7592764C>G	GRCh37
NC_000019.8:g.7498764C>G	NCBI36
NG_015806.1:g.10269C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.695C>G MANE Select	ENSP00000264079.5:p.Thr232Ser
ENST00000264079.10:c.695C>G	ENSP00000264079.5:p.Thr232Ser
ENST00000394321.9:n.1010C>G
ENST00000601003.1:c.586C>G	ENSP00000469074.1:p.Pro196Ala
NM_020533.2:c.695C>G	NP_065394.1:p.Thr232Ser
NM_020533.3:c.695C>G MANE Select	NP_065394.1:p.Thr232Ser