Canonical Allele Identifier: CA2587948323
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7527490-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527490T>G , CM000681.2:g.7527490T>G GRCh38
NC_000019.9:g.7592376T>G , CM000681.1:g.7592376T>G GRCh37
NC_000019.8:g.7498376T>G NCBI36
NG_015806.1:g.9881T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.572-30T>G MANE Select ENSP00000264079.5:n.572-30T>G
ENST00000264079.10:c.572-30T>G ENSP00000264079.5:n.572-30T>G
ENST00000394321.9:n.652-30T>G
ENST00000598406.1:n.393-30T>G
ENST00000601003.1:c.572-374T>G ENSP00000469074.1:n.572-374T>G
NM_020533.2:c.572-30T>G NP_065394.1:n.572-30T>G
NM_020533.3:c.572-30T>G MANE Select NP_065394.1:n.572-30T>G