Canonical Allele Identifier: CA2320962381
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527581C= , CM000681.2:g.7527581C= GRCh38
NC_000019.9:g.7592467C= , CM000681.1:g.7592467C= GRCh37
NC_000019.8:g.7498467C= NCBI36
NG_015806.1:g.9972C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.633C= MANE Select ENSP00000264079.5:p.Leu211=
ENST00000264079.10:c.633C= ENSP00000264079.5:p.Leu211=
ENST00000394321.9:n.713C=
ENST00000598406.1:n.454C=
ENST00000601003.1:c.572-283C= ENSP00000469074.1:n.572-283C=
NM_020533.2:c.633C= NP_065394.1:p.Leu211=
NM_020533.3:c.633C= MANE Select NP_065394.1:p.Leu211=