Canonical Allele Identifier: CA403080796
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526509A>T , CM000681.2:g.7526509A>T GRCh38
NC_000019.9:g.7591395A>T , CM000681.1:g.7591395A>T GRCh37
NC_000019.8:g.7497395A>T NCBI36
NG_015806.1:g.8900A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.308A>T MANE Select ENSP00000264079.5:p.His103Leu
ENST00000264079.10:c.308A>T ENSP00000264079.5:p.His103Leu
ENST00000394321.9:n.388A>T
ENST00000596008.1:n.270A>T
ENST00000598406.1:n.129A>T
ENST00000601003.1:c.308A>T ENSP00000469074.1:p.His103Leu
NM_020533.2:c.308A>T NP_065394.1:p.His103Leu
NM_020533.3:c.308A>T MANE Select NP_065394.1:p.His103Leu