Canonical Allele Identifier: CA403153006
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525153T>C , CM000681.2:g.7525153T>C GRCh38
NC_000019.9:g.7590039T>C , CM000681.1:g.7590039T>C GRCh37
NC_000019.8:g.7496039T>C NCBI36
NG_015806.1:g.7544T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.224T>C MANE Select ENSP00000264079.5:p.Val75Ala
ENST00000264079.10:c.224T>C ENSP00000264079.5:p.Val75Ala
ENST00000394321.9:n.304T>C
ENST00000596390.1:n.340T>C
ENST00000601003.1:c.224T>C ENSP00000469074.1:p.Val75Ala
NM_020533.2:c.224T>C NP_065394.1:p.Val75Ala
NM_020533.3:c.224T>C MANE Select NP_065394.1:p.Val75Ala