Canonical Allele Identifier: CA631318848
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1210781690
gnomAD v2: 19-7595007-C-G
gnomAD v3: 19-7530121-C-G
gnomAD v4: 19-7530121-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530121C>G , CM000681.2:g.7530121C>G GRCh38
NC_000019.9:g.7595007C>G , CM000681.1:g.7595007C>G GRCh37
NC_000019.8:g.7501007C>G NCBI36
NG_013374.1:g.970C>G
NG_015806.1:g.12512C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1360-165C>G MANE Select ENSP00000264079.5:n.1360-165C>G
ENST00000264079.10:c.1360-165C>G ENSP00000264079.5:n.1360-165C>G
ENST00000394321.9:n.1675-165C>G
ENST00000594692.1:n.356-165C>G
ENST00000595860.5:n.543-165C>G
ENST00000599334.1:c.237-314C>G
NM_020533.2:c.1360-165C>G NP_065394.1:n.1360-165C>G
NM_020533.3:c.1360-165C>G MANE Select NP_065394.1:n.1360-165C>G