Canonical Allele Identifier: CA884198518

Gene: MCOLN1

Linked Data

• dbSNP Id: rs1198834123
• gnomAD v3: 19-7524862-G-C
• gnomAD v4: 19-7524862-G-C
• MyVariant Identifiers: chr19:g.7589748G>C (hg19) ; chr19:g.7524862G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7524862G>C , CM000681.2:g.7524862G>C	GRCh38
NC_000019.9:g.7589748G>C , CM000681.1:g.7589748G>C	GRCh37
NC_000019.8:g.7495748G>C	NCBI36
NG_015806.1:g.7253G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.32-99G>C MANE Select	ENSP00000264079.5:n.32-99G>C
ENST00000264079.10:c.32-99G>C	ENSP00000264079.5:n.32-99G>C
ENST00000394321.9:n.112-99G>C
ENST00000596390.1:n.148-99G>C
ENST00000601003.1:c.32-99G>C	ENSP00000469074.1:n.32-99G>C
NM_020533.2:c.32-99G>C	NP_065394.1:n.32-99G>C
XR_936293.1:n.93C>G
XR_936294.1:n.93C>G
XR_936295.1:n.93C>G
XR_936293.2:n.119C>G
XR_936294.2:n.119C>G
NM_020533.3:c.32-99G>C MANE Select	NP_065394.1:n.32-99G>C