Canonical Allele Identifier: CA2739637887
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527767G>C , CM000681.2:g.7527767G>C GRCh38
NC_000019.9:g.7592653G>C , CM000681.1:g.7592653G>C GRCh37
NC_000019.8:g.7498653G>C NCBI36
NG_015806.1:g.10158G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.681-97G>C MANE Select ENSP00000264079.5:n.681-97G>C
ENST00000264079.10:c.681-97G>C ENSP00000264079.5:n.681-97G>C
ENST00000394321.9:n.899G>C
ENST00000598406.1:n.640G>C
ENST00000601003.1:c.572-97G>C ENSP00000469074.1:n.572-97G>C
NM_020533.2:c.681-97G>C NP_065394.1:n.681-97G>C
NM_020533.3:c.681-97G>C MANE Select NP_065394.1:n.681-97G>C
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Search 100 bp 3'