Canonical Allele Identifier: CA2320960171
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7522792G= , CM000681.2:g.7522792G= GRCh38
NC_000019.9:g.7587678G= , CM000681.1:g.7587678G= GRCh37
NC_000019.8:g.7493678G= NCBI36
NG_015806.1:g.5183G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.31+11G= MANE Select ENSP00000264079.5:n.31+11G=
ENST00000264079.10:c.31+11G= ENSP00000264079.5:n.31+11G=
ENST00000394321.9:n.111+11G=
ENST00000596390.1:n.147+11G=
ENST00000601003.1:c.31+11G= ENSP00000469074.1:n.31+11G=
NM_020533.2:c.31+11G= NP_065394.1:n.31+11G=
XR_936293.1:n.926+50C=
XR_936294.1:n.926+50C=
XR_936295.1:n.570+50C=
XR_936293.2:n.952+50C=
XR_936294.2:n.952+50C=
NM_020533.3:c.31+11G= MANE Select NP_065394.1:n.31+11G=