Canonical Allele Identifier: CA2510602964
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526652G>T , CM000681.2:g.7526652G>T GRCh38
NC_000019.9:g.7591538G>T , CM000681.1:g.7591538G>T GRCh37
NC_000019.8:g.7497538G>T NCBI36
NG_015806.1:g.9043G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.405+46G>T MANE Select ENSP00000264079.5:n.405+46G>T
ENST00000264079.10:c.405+46G>T ENSP00000264079.5:n.405+46G>T
ENST00000394321.9:n.485+46G>T
ENST00000596008.1:n.367+46G>T
ENST00000598406.1:n.226+46G>T
ENST00000601003.1:c.405+46G>T ENSP00000469074.1:n.405+46G>T
NM_020533.2:c.405+46G>T NP_065394.1:n.405+46G>T
NM_020533.3:c.405+46G>T MANE Select NP_065394.1:n.405+46G>T