Canonical Allele Identifier: CA2320965312
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533574C= , CM000681.2:g.7533574C= GRCh38
NC_000019.9:g.7598460C= , CM000681.1:g.7598460C= GRCh37
NC_000019.8:g.7504460C= NCBI36
NG_013374.1:g.4423C=
NG_015806.1:g.15965C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1627C= MANE Select ENSP00000264079.5:p.Gln543=
ENST00000264079.10:c.1627C= ENSP00000264079.5:p.Gln543=
ENST00000394321.9:n.1942C=
ENST00000599334.1:c.355C=
ENST00000602227.1:n.181C=
NM_020533.2:c.1627C= NP_065394.1:p.Gln543=
NM_020533.3:c.1627C= MANE Select NP_065394.1:p.Gln543=