Canonical Allele Identifier: CA2587948455
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527788_7527789insCCCT , CM000681.2:g.7527788_7527789insCCCT GRCh38
NC_000019.9:g.7592674_7592675insCCCT , CM000681.1:g.7592674_7592675insCCCT GRCh37
NC_000019.8:g.7498674_7498675insCCCT NCBI36
NG_015806.1:g.10179_10180insCCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.681-76_681-75insCCCT MANE Select ENSP00000264079.5:n.681-76_681-75insCCCT
ENST00000264079.10:c.681-76_681-75insCCCT ENSP00000264079.5:n.681-76_681-75insCCCT
ENST00000394321.9:n.920_921insCCCT
ENST00000601003.1:c.572-76_572-75insCCCT ENSP00000469074.1:n.572-76_572-75insCCCT
NM_020533.2:c.681-76_681-75insCCCT NP_065394.1:n.681-76_681-75insCCCT
NM_020533.3:c.681-76_681-75insCCCT MANE Select NP_065394.1:n.681-76_681-75insCCCT