Canonical Allele Identifier: CA2320962962
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528755C= , CM000681.2:g.7528755C= GRCh38
NC_000019.9:g.7593641C= , CM000681.1:g.7593641C= GRCh37
NC_000019.8:g.7499641C= NCBI36
NG_015806.1:g.11146C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.984+52C= MANE Select ENSP00000264079.5:n.984+52C=
ENST00000264079.10:c.984+52C= ENSP00000264079.5:n.984+52C=
ENST00000394321.9:n.1299+52C=
ENST00000595860.5:n.102C=
NM_020533.2:c.984+52C= NP_065394.1:n.984+52C=
NM_020533.3:c.984+52C= MANE Select NP_065394.1:n.984+52C=