Canonical Allele Identifier: CA2587949563
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7530227-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530227C>A , CM000681.2:g.7530227C>A GRCh38
NC_000019.9:g.7595113C>A , CM000681.1:g.7595113C>A GRCh37
NC_000019.8:g.7501113C>A NCBI36
NG_013374.1:g.1076C>A
NG_015806.1:g.12618C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-59C>A MANE Select ENSP00000264079.5:n.1360-59C>A
ENST00000264079.10:c.1360-59C>A ENSP00000264079.5:n.1360-59C>A
ENST00000394321.9:n.1675-59C>A
ENST00000594692.1:n.356-59C>A
ENST00000595860.5:n.543-59C>A
ENST00000599334.1:c.237-208C>A
NM_020533.2:c.1360-59C>A NP_065394.1:n.1360-59C>A
NM_020533.3:c.1360-59C>A MANE Select NP_065394.1:n.1360-59C>A