Canonical Allele Identifier: CA2320961011

Gene: MCOLN1

Linked Data

• dbSNP Id: rs1599252033

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7524746A>C , CM000681.2:g.7524746A>C	GRCh38
NC_000019.9:g.7589632A>C , CM000681.1:g.7589632A>C	GRCh37
NC_000019.8:g.7495632A>C	NCBI36
NG_015806.1:g.7137A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264079.11:c.32-215A>C MANE Select	ENSP00000264079.5:n.32-215A>C
ENST00000264079.10:c.32-215A>C	ENSP00000264079.5:n.32-215A>C
ENST00000394321.9:n.112-215A>C
ENST00000596390.1:n.148-215A>C
ENST00000601003.1:c.32-215A>C	ENSP00000469074.1:n.32-215A>C
NM_020533.2:c.32-215A>C	NP_065394.1:n.32-215A>C
XR_936293.1:n.209T>G
XR_936294.1:n.209T>G
XR_936295.1:n.154+55T>G
XR_936293.2:n.235T>G
XR_936294.2:n.235T>G
NM_020533.3:c.32-215A>C MANE Select	NP_065394.1:n.32-215A>C