Canonical Allele Identifier: CA2587949566
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7530229-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530229A>G , CM000681.2:g.7530229A>G GRCh38
NC_000019.9:g.7595115A>G , CM000681.1:g.7595115A>G GRCh37
NC_000019.8:g.7501115A>G NCBI36
NG_013374.1:g.1078A>G
NG_015806.1:g.12620A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-57A>G MANE Select ENSP00000264079.5:n.1360-57A>G
ENST00000264079.10:c.1360-57A>G ENSP00000264079.5:n.1360-57A>G
ENST00000394321.9:n.1675-57A>G
ENST00000594692.1:n.356-57A>G
ENST00000595860.5:n.543-57A>G
ENST00000599334.1:c.237-206A>G
NM_020533.2:c.1360-57A>G NP_065394.1:n.1360-57A>G
NM_020533.3:c.1360-57A>G MANE Select NP_065394.1:n.1360-57A>G