Canonical Allele Identifier: CA403082096
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7527555-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527555C>G , CM000681.2:g.7527555C>G GRCh38
NC_000019.9:g.7592441C>G , CM000681.1:g.7592441C>G GRCh37
NC_000019.8:g.7498441C>G NCBI36
NG_015806.1:g.9946C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.607C>G MANE Select ENSP00000264079.5:p.Pro203Ala
ENST00000264079.10:c.607C>G ENSP00000264079.5:p.Pro203Ala
ENST00000394321.9:n.687C>G
ENST00000598406.1:n.428C>G
ENST00000601003.1:c.572-309C>G ENSP00000469074.1:n.572-309C>G
NM_020533.2:c.607C>G NP_065394.1:p.Pro203Ala
NM_020533.3:c.607C>G MANE Select NP_065394.1:p.Pro203Ala