Canonical Allele Identifier: CA403080786
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526504C>G , CM000681.2:g.7526504C>G GRCh38
NC_000019.9:g.7591390C>G , CM000681.1:g.7591390C>G GRCh37
NC_000019.8:g.7497390C>G NCBI36
NG_015806.1:g.8895C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.303C>G MANE Select ENSP00000264079.5:p.Phe101Leu
ENST00000264079.10:c.303C>G ENSP00000264079.5:p.Phe101Leu
ENST00000394321.9:n.383C>G
ENST00000596008.1:n.265C>G
ENST00000598406.1:n.124C>G
ENST00000601003.1:c.303C>G ENSP00000469074.1:p.Phe101Leu
NM_020533.2:c.303C>G NP_065394.1:p.Phe101Leu
NM_020533.3:c.303C>G MANE Select NP_065394.1:p.Phe101Leu