Canonical Allele Identifier: CA403091486
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533567C>G , CM000681.2:g.7533567C>G GRCh38
NC_000019.9:g.7598453C>G , CM000681.1:g.7598453C>G GRCh37
NC_000019.8:g.7504453C>G NCBI36
NG_013374.1:g.4416C>G
NG_015806.1:g.15958C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1620C>G MANE Select ENSP00000264079.5:p.Tyr540Ter
ENST00000264079.10:c.1620C>G ENSP00000264079.5:p.Tyr540Ter
ENST00000394321.9:n.1935C>G
ENST00000599334.1:c.348C>G
ENST00000602227.1:n.174C>G
NM_020533.2:c.1620C>G NP_065394.1:p.Tyr540Ter
NM_020533.3:c.1620C>G MANE Select NP_065394.1:p.Tyr540Ter