Canonical Allele Identifier: CA884198462

Gene: MCOLN1

Linked Data

• dbSNP Id: rs1408398548
• MyVariant Identifiers: chr19:g.7589591A>T (hg19) ; chr19:g.7524705A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7524705A>T , CM000681.2:g.7524705A>T	GRCh38
NC_000019.9:g.7589591A>T , CM000681.1:g.7589591A>T	GRCh37
NC_000019.8:g.7495591A>T	NCBI36
NG_015806.1:g.7096A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.32-256A>T MANE Select	ENSP00000264079.5:n.32-256A>T
ENST00000264079.10:c.32-256A>T	ENSP00000264079.5:n.32-256A>T
ENST00000394321.9:n.112-256A>T
ENST00000596390.1:n.148-256A>T
ENST00000601003.1:c.32-256A>T	ENSP00000469074.1:n.32-256A>T
NM_020533.2:c.32-256A>T	NP_065394.1:n.32-256A>T
XR_936293.1:n.250T>A
XR_936294.1:n.250T>A
XR_936295.1:n.154+96T>A
XR_936293.2:n.276T>A
XR_936294.2:n.276T>A
NM_020533.3:c.32-256A>T MANE Select	NP_065394.1:n.32-256A>T