Canonical Allele Identifier: CA2320963780
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530314G= , CM000681.2:g.7530314G= GRCh38
NC_000019.9:g.7595200G= , CM000681.1:g.7595200G= GRCh37
NC_000019.8:g.7501200G= NCBI36
NG_013374.1:g.1163G=
NG_015806.1:g.12705G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1388G= MANE Select ENSP00000264079.5:p.Cys463=
ENST00000264079.10:c.1388G= ENSP00000264079.5:p.Cys463=
ENST00000394321.9:n.1703G=
ENST00000594692.1:n.384G=
ENST00000595860.5:n.571G=
ENST00000599334.1:c.237-121G=
NM_020533.2:c.1388G= NP_065394.1:p.Cys463=
NM_020533.3:c.1388G= MANE Select NP_065394.1:p.Cys463=