Canonical Allele Identifier: CA403081529
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526863T>G , CM000681.2:g.7526863T>G GRCh38
NC_000019.9:g.7591749T>G , CM000681.1:g.7591749T>G GRCh37
NC_000019.8:g.7497749T>G NCBI36
NG_015806.1:g.9254T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.508T>G MANE Select ENSP00000264079.5:p.Tyr170Asp
ENST00000264079.10:c.508T>G ENSP00000264079.5:p.Tyr170Asp
ENST00000394321.9:n.588T>G
ENST00000596008.1:n.470T>G
ENST00000598406.1:n.329T>G
ENST00000601003.1:c.508T>G ENSP00000469074.1:p.Tyr170Asp
NM_020533.2:c.508T>G NP_065394.1:p.Tyr170Asp
NM_020533.3:c.508T>G MANE Select NP_065394.1:p.Tyr170Asp