Canonical Allele Identifier: CA2813475800
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530233C>T , CM000681.2:g.7530233C>T GRCh38
NC_000019.9:g.7595119C>T , CM000681.1:g.7595119C>T GRCh37
NC_000019.8:g.7501119C>T NCBI36
NG_013374.1:g.1082C>T
NG_015806.1:g.12624C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-53C>T MANE Select ENSP00000264079.5:n.1360-53C>T
ENST00000264079.10:c.1360-53C>T ENSP00000264079.5:n.1360-53C>T
ENST00000394321.9:n.1675-53C>T
ENST00000594692.1:n.356-53C>T
ENST00000595860.5:n.543-53C>T
ENST00000599334.1:c.237-202C>T
NM_020533.2:c.1360-53C>T NP_065394.1:n.1360-53C>T
NM_020533.3:c.1360-53C>T MANE Select NP_065394.1:n.1360-53C>T