Canonical Allele Identifier: CA2320963707
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1599255980
gnomAD v4: 19-7530152-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530152A>G , CM000681.2:g.7530152A>G GRCh38
NC_000019.9:g.7595038A>G , CM000681.1:g.7595038A>G GRCh37
NC_000019.8:g.7501038A>G NCBI36
NG_013374.1:g.1001A>G
NG_015806.1:g.12543A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1360-134A>G MANE Select ENSP00000264079.5:n.1360-134A>G
ENST00000264079.10:c.1360-134A>G ENSP00000264079.5:n.1360-134A>G
ENST00000394321.9:n.1675-134A>G
ENST00000594692.1:n.356-134A>G
ENST00000595860.5:n.543-134A>G
ENST00000599334.1:c.237-283A>G
NM_020533.2:c.1360-134A>G NP_065394.1:n.1360-134A>G
NM_020533.3:c.1360-134A>G MANE Select NP_065394.1:n.1360-134A>G