Canonical Allele Identifier: CA631318850
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1292534135
gnomAD v2: 19-7595008-C-G
gnomAD v3: 19-7530122-C-G
gnomAD v4: 19-7530122-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530122C>G , CM000681.2:g.7530122C>G GRCh38
NC_000019.9:g.7595008C>G , CM000681.1:g.7595008C>G GRCh37
NC_000019.8:g.7501008C>G NCBI36
NG_013374.1:g.971C>G
NG_015806.1:g.12513C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1360-164C>G MANE Select ENSP00000264079.5:n.1360-164C>G
ENST00000264079.10:c.1360-164C>G ENSP00000264079.5:n.1360-164C>G
ENST00000394321.9:n.1675-164C>G
ENST00000594692.1:n.356-164C>G
ENST00000595860.5:n.543-164C>G
ENST00000599334.1:c.237-313C>G
NM_020533.2:c.1360-164C>G NP_065394.1:n.1360-164C>G
NM_020533.3:c.1360-164C>G MANE Select NP_065394.1:n.1360-164C>G