Canonical Allele Identifier: CA403081934

Gene: MCOLN1

Linked Data

• dbSNP Id: rs577440930
• MyVariant Identifiers: chr19:g.7592417G>T (hg19) ; chr19:g.7527531G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7527531G>T , CM000681.2:g.7527531G>T	GRCh38
NC_000019.9:g.7592417G>T , CM000681.1:g.7592417G>T	GRCh37
NC_000019.8:g.7498417G>T	NCBI36
NG_015806.1:g.9922G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.583G>T MANE Select	ENSP00000264079.5:p.Val195Leu
ENST00000264079.10:c.583G>T	ENSP00000264079.5:p.Val195Leu
ENST00000394321.9:n.663G>T
ENST00000598406.1:n.404G>T
ENST00000601003.1:c.572-333G>T	ENSP00000469074.1:n.572-333G>T
NM_020533.2:c.583G>T	NP_065394.1:p.Val195Leu
NM_020533.3:c.583G>T MANE Select	NP_065394.1:p.Val195Leu