Canonical Allele Identifier: CA2320963776
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530301A= , CM000681.2:g.7530301A= GRCh38
NC_000019.9:g.7595187A= , CM000681.1:g.7595187A= GRCh37
NC_000019.8:g.7501187A= NCBI36
NG_013374.1:g.1150A=
NG_015806.1:g.12692A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1375A= MANE Select ENSP00000264079.5:p.Met459=
ENST00000264079.10:c.1375A= ENSP00000264079.5:p.Met459=
ENST00000394321.9:n.1690A=
ENST00000594692.1:n.371A=
ENST00000595860.5:n.558A=
ENST00000599334.1:c.237-134A=
NM_020533.2:c.1375A= NP_065394.1:p.Met459=
NM_020533.3:c.1375A= MANE Select NP_065394.1:p.Met459=