Canonical Allele Identifier: CA403091979
Gene: MCOLN1 HGNC NCBI

Linked Data

COSMIC: COSM440631
MyVariant Identifiers: chr19:g.7598649C>G (hg19) chr19:g.7533763C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533763C>G , CM000681.2:g.7533763C>G GRCh38
NC_000019.9:g.7598649C>G , CM000681.1:g.7598649C>G GRCh37
NC_000019.8:g.7504649C>G NCBI36
NG_013374.1:g.4612C>G
NG_015806.1:g.16154C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1711C>G MANE Select ENSP00000264079.5:p.Pro571Ala
ENST00000264079.10:c.1711C>G ENSP00000264079.5:p.Pro571Ala
ENST00000394321.9:n.2026C>G
ENST00000599334.1:c.439C>G
ENST00000601870.1:c.64C>G
ENST00000602227.1:n.265C>G
NM_020533.2:c.1711C>G NP_065394.1:p.Pro571Ala
NM_020533.3:c.1711C>G MANE Select NP_065394.1:p.Pro571Ala
Search 100 bp 5'
Search 100 bp 3'