Canonical Allele Identifier: CA2320965661
Gene: MCOLN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533980G= , CM000681.2:g.7533980G= GRCh38
NC_000019.9:g.7598866G= , CM000681.1:g.7598866G= GRCh37
NC_000019.8:g.7504866G= NCBI36
NG_013374.1:g.4829G=
NG_015806.1:g.16371G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*185G= MANE Select ENSP00000264079.5:n.*185G=
ENST00000264079.10:c.*185G= ENSP00000264079.5:n.*185G=
ENST00000394321.9:n.2243G=
ENST00000599334.1:c.656G=
ENST00000601870.1:c.169+112G=
ENST00000602227.1:n.482G=
NM_020533.2:c.*185G= NP_065394.1:n.*185G=
NM_020533.3:c.*185G= MANE Select NP_065394.1:n.*185G=
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