Canonical Allele Identifier: CA2320965321
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533584A= , CM000681.2:g.7533584A= GRCh38
NC_000019.9:g.7598470A= , CM000681.1:g.7598470A= GRCh37
NC_000019.8:g.7504470A= NCBI36
NG_013374.1:g.4433A=
NG_015806.1:g.15975A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1637A= MANE Select ENSP00000264079.5:p.Asp546=
ENST00000264079.10:c.1637A= ENSP00000264079.5:p.Asp546=
ENST00000394321.9:n.1952A=
ENST00000599334.1:c.365A=
ENST00000602227.1:n.191A=
NM_020533.2:c.1637A= NP_065394.1:p.Asp546=
NM_020533.3:c.1637A= MANE Select NP_065394.1:p.Asp546=