Canonical Allele Identifier: CA2576596942
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526984A>T , CM000681.2:g.7526984A>T GRCh38
NC_000019.9:g.7591870A>T , CM000681.1:g.7591870A>T GRCh37
NC_000019.8:g.7497870A>T NCBI36
NG_015806.1:g.9375A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.571+58A>T MANE Select ENSP00000264079.5:n.571+58A>T
ENST00000264079.10:c.571+58A>T ENSP00000264079.5:n.571+58A>T
ENST00000394321.9:n.651+58A>T
ENST00000596008.1:n.591A>T
ENST00000598406.1:n.392+58A>T
ENST00000601003.1:c.571+58A>T ENSP00000469074.1:n.571+58A>T
NM_020533.2:c.571+58A>T NP_065394.1:n.571+58A>T
NM_020533.3:c.571+58A>T MANE Select NP_065394.1:n.571+58A>T