Canonical Allele Identifier: CA2320963042

Gene: MCOLN1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7528916C= , CM000681.2:g.7528916C=	GRCh38
NC_000019.9:g.7593802C= , CM000681.1:g.7593802C=	GRCh37
NC_000019.8:g.7499802C=	NCBI36
NG_015806.1:g.11307C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264079.11:c.1080C= MANE Select	ENSP00000264079.5:p.Thr360=
ENST00000264079.10:c.1080C=	ENSP00000264079.5:p.Thr360=
ENST00000394321.9:n.1395C=
ENST00000595860.5:n.263C=
NM_020533.2:c.1080C=	NP_065394.1:p.Thr360=
NM_020533.3:c.1080C= MANE Select	NP_065394.1:p.Thr360=