Canonical Allele Identifier: CA403086132

Gene: MCOLN1

Linked Data

• MyVariant Identifiers: chr19:g.7593803A>T (hg19) ; chr19:g.7528917A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7528917A>T , CM000681.2:g.7528917A>T	GRCh38
NC_000019.9:g.7593803A>T , CM000681.1:g.7593803A>T	GRCh37
NC_000019.8:g.7499803A>T	NCBI36
NG_015806.1:g.11308A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264079.11:c.1081A>T MANE Select	ENSP00000264079.5:p.Ser361Cys
ENST00000264079.10:c.1081A>T	ENSP00000264079.5:p.Ser361Cys
ENST00000394321.9:n.1396A>T
ENST00000595860.5:n.264A>T
NM_020533.2:c.1081A>T	NP_065394.1:p.Ser361Cys
NM_020533.3:c.1081A>T MANE Select	NP_065394.1:p.Ser361Cys