Canonical Allele Identifier: CA2320962223
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527270_7527271delinsTC , CM000681.2:g.7527270_7527271delinsTC GRCh38
NC_000019.9:g.7592156_7592157delinsTC , CM000681.1:g.7592156_7592157delinsTC GRCh37
NC_000019.8:g.7498156_7498157delinsTC NCBI36
NG_015806.1:g.9661_9662delinsTC

Transcript Alleles

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