Canonical Allele Identifier: CA2813475775
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530115C>T , CM000681.2:g.7530115C>T GRCh38
NC_000019.9:g.7595001C>T , CM000681.1:g.7595001C>T GRCh37
NC_000019.8:g.7501001C>T NCBI36
NG_013374.1:g.964C>T
NG_015806.1:g.12506C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1360-171C>T MANE Select ENSP00000264079.5:n.1360-171C>T
ENST00000264079.10:c.1360-171C>T ENSP00000264079.5:n.1360-171C>T
ENST00000394321.9:n.1675-171C>T
ENST00000594692.1:n.356-171C>T
ENST00000595860.5:n.543-171C>T
ENST00000599334.1:c.237-320C>T
NM_020533.2:c.1360-171C>T NP_065394.1:n.1360-171C>T
NM_020533.3:c.1360-171C>T MANE Select NP_065394.1:n.1360-171C>T