Canonical Allele Identifier: CA2587949558
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7530222-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530222T>G , CM000681.2:g.7530222T>G GRCh38
NC_000019.9:g.7595108T>G , CM000681.1:g.7595108T>G GRCh37
NC_000019.8:g.7501108T>G NCBI36
NG_013374.1:g.1071T>G
NG_015806.1:g.12613T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-64T>G MANE Select ENSP00000264079.5:n.1360-64T>G
ENST00000264079.10:c.1360-64T>G ENSP00000264079.5:n.1360-64T>G
ENST00000394321.9:n.1675-64T>G
ENST00000594692.1:n.356-64T>G
ENST00000595860.5:n.543-64T>G
ENST00000599334.1:c.237-213T>G
NM_020533.2:c.1360-64T>G NP_065394.1:n.1360-64T>G
NM_020533.3:c.1360-64T>G MANE Select NP_065394.1:n.1360-64T>G