Canonical Allele Identifier: CA2582317568
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527270_7527271insAAAA , CM000681.2:g.7527270_7527271insAAAA GRCh38
NC_000019.9:g.7592156_7592157insAAAA , CM000681.1:g.7592156_7592157insAAAA GRCh37
NC_000019.8:g.7498156_7498157insAAAA NCBI36
NG_015806.1:g.9661_9662insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.572-250_572-249insAAAA MANE Select ENSP00000264079.5:n.572-250_572-249insAAAA
ENST00000264079.10:c.572-250_572-249insAAAA ENSP00000264079.5:n.572-250_572-249insAAAA
ENST00000394321.9:n.652-250_652-249insAAAA
ENST00000598406.1:n.393-250_393-249insAAAA
ENST00000601003.1:c.571+344_571+345insAAAA ENSP00000469074.1:n.571+344_571+345insAAAA
NM_020533.2:c.572-250_572-249insAAAA NP_065394.1:n.572-250_572-249insAAAA
NM_020533.3:c.572-250_572-249insAAAA MANE Select NP_065394.1:n.572-250_572-249insAAAA