Canonical Allele Identifier: CA403089659
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530382C>G , CM000681.2:g.7530382C>G GRCh38
NC_000019.9:g.7595268C>G , CM000681.1:g.7595268C>G GRCh37
NC_000019.8:g.7501268C>G NCBI36
NG_013374.1:g.1231C>G
NG_015806.1:g.12773C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1456C>G MANE Select ENSP00000264079.5:p.Arg486Gly
ENST00000264079.10:c.1456C>G ENSP00000264079.5:p.Arg486Gly
ENST00000394321.9:n.1771C>G
ENST00000594692.1:n.452C>G
ENST00000595860.5:n.639C>G
ENST00000599334.1:c.237-53C>G
NM_020533.2:c.1456C>G NP_065394.1:p.Arg486Gly
NM_020533.3:c.1456C>G MANE Select NP_065394.1:p.Arg486Gly