Canonical Allele Identifier: CA2320963751
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530242T= , CM000681.2:g.7530242T= GRCh38
NC_000019.9:g.7595128T= , CM000681.1:g.7595128T= GRCh37
NC_000019.8:g.7501128T= NCBI36
NG_013374.1:g.1091T=
NG_015806.1:g.12633T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-44T= MANE Select ENSP00000264079.5:n.1360-44T=
ENST00000264079.10:c.1360-44T= ENSP00000264079.5:n.1360-44T=
ENST00000394321.9:n.1675-44T=
ENST00000594692.1:n.356-44T=
ENST00000595860.5:n.543-44T=
ENST00000599334.1:c.237-193T=
NM_020533.2:c.1360-44T= NP_065394.1:n.1360-44T=
NM_020533.3:c.1360-44T= MANE Select NP_065394.1:n.1360-44T=