Canonical Allele Identifier: CA2320963750
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530240C= , CM000681.2:g.7530240C= GRCh38
NC_000019.9:g.7595126C= , CM000681.1:g.7595126C= GRCh37
NC_000019.8:g.7501126C= NCBI36
NG_013374.1:g.1089C=
NG_015806.1:g.12631C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-46C= MANE Select ENSP00000264079.5:n.1360-46C=
ENST00000264079.10:c.1360-46C= ENSP00000264079.5:n.1360-46C=
ENST00000394321.9:n.1675-46C=
ENST00000594692.1:n.356-46C=
ENST00000595860.5:n.543-46C=
ENST00000599334.1:c.237-195C=
NM_020533.2:c.1360-46C= NP_065394.1:n.1360-46C=
NM_020533.3:c.1360-46C= MANE Select NP_065394.1:n.1360-46C=