Canonical Allele Identifier: CA403084909
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1428466963
gnomAD v2: 19-7593126-C-T
gnomAD v4: 19-7528240-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528240C>T , CM000681.2:g.7528240C>T GRCh38
NC_000019.9:g.7593126C>T , CM000681.1:g.7593126C>T GRCh37
NC_000019.8:g.7499126C>T NCBI36
NG_015806.1:g.10631C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.860C>T MANE Select ENSP00000264079.5:p.Pro287Leu
ENST00000264079.10:c.860C>T ENSP00000264079.5:p.Pro287Leu
ENST00000394321.9:n.1175C>T
NM_020533.2:c.860C>T NP_065394.1:p.Pro287Leu
NM_020533.3:c.860C>T MANE Select NP_065394.1:p.Pro287Leu