Canonical Allele Identifier: CA2739637885
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527766T>G , CM000681.2:g.7527766T>G GRCh38
NC_000019.9:g.7592652T>G , CM000681.1:g.7592652T>G GRCh37
NC_000019.8:g.7498652T>G NCBI36
NG_015806.1:g.10157T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-98T>G MANE Select ENSP00000264079.5:n.681-98T>G
ENST00000264079.10:c.681-98T>G ENSP00000264079.5:n.681-98T>G
ENST00000394321.9:n.898T>G
ENST00000598406.1:n.639T>G
ENST00000601003.1:c.572-98T>G ENSP00000469074.1:n.572-98T>G
NM_020533.2:c.681-98T>G NP_065394.1:n.681-98T>G
NM_020533.3:c.681-98T>G MANE Select NP_065394.1:n.681-98T>G