Canonical Allele Identifier: CA304894464

Gene: MCOLN1

Linked Data

• dbSNP Id: rs138579701
• gnomAD v2: 19-7589687-A-G
• gnomAD v3: 19-7524801-A-G
• gnomAD v4: 19-7524801-A-G
• MyVariant Identifiers: chr19:g.7589687A>G (hg19) ; chr19:g.7524801A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7524801A>G , CM000681.2:g.7524801A>G	GRCh38
NC_000019.9:g.7589687A>G , CM000681.1:g.7589687A>G	GRCh37
NC_000019.8:g.7495687A>G	NCBI36
NG_015806.1:g.7192A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.32-160A>G MANE Select	ENSP00000264079.5:n.32-160A>G
ENST00000264079.10:c.32-160A>G	ENSP00000264079.5:n.32-160A>G
ENST00000394321.9:n.112-160A>G
ENST00000596390.1:n.148-160A>G
ENST00000601003.1:c.32-160A>G	ENSP00000469074.1:n.32-160A>G
NM_020533.2:c.32-160A>G	NP_065394.1:n.32-160A>G
XR_936293.1:n.154T>C
XR_936294.1:n.154T>C
XR_936295.1:n.154T>C
XR_936293.2:n.180T>C
XR_936294.2:n.180T>C
NM_020533.3:c.32-160A>G MANE Select	NP_065394.1:n.32-160A>G