Canonical Allele Identifier: CA2739637925
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527794G>T , CM000681.2:g.7527794G>T GRCh38
NC_000019.9:g.7592680G>T , CM000681.1:g.7592680G>T GRCh37
NC_000019.8:g.7498680G>T NCBI36
NG_015806.1:g.10185G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-70G>T MANE Select ENSP00000264079.5:n.681-70G>T
ENST00000264079.10:c.681-70G>T ENSP00000264079.5:n.681-70G>T
ENST00000394321.9:n.926G>T
ENST00000601003.1:c.572-70G>T ENSP00000469074.1:n.572-70G>T
NM_020533.2:c.681-70G>T NP_065394.1:n.681-70G>T
NM_020533.3:c.681-70G>T MANE Select NP_065394.1:n.681-70G>T
Search 100 bp 5'
Search 100 bp 3'