Canonical Allele Identifier: CA2320963631
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530035C= , CM000681.2:g.7530035C= GRCh38
NC_000019.9:g.7594921C= , CM000681.1:g.7594921C= GRCh37
NC_000019.8:g.7500921C= NCBI36
NG_013374.1:g.884C=
NG_015806.1:g.12426C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1360-251C= MANE Select ENSP00000264079.5:n.1360-251C=
ENST00000264079.10:c.1360-251C= ENSP00000264079.5:n.1360-251C=
ENST00000394321.9:n.1675-251C=
ENST00000594692.1:n.356-251C=
ENST00000595860.5:n.543-251C=
ENST00000599334.1:c.236+323C=
NM_020533.2:c.1360-251C= NP_065394.1:n.1360-251C=
NM_020533.3:c.1360-251C= MANE Select NP_065394.1:n.1360-251C=
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