Canonical Allele Identifier: CA2576596920
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7526654-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526654C>A , CM000681.2:g.7526654C>A GRCh38
NC_000019.9:g.7591540C>A , CM000681.1:g.7591540C>A GRCh37
NC_000019.8:g.7497540C>A NCBI36
NG_015806.1:g.9045C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.405+48C>A MANE Select ENSP00000264079.5:n.405+48C>A
ENST00000264079.10:c.405+48C>A ENSP00000264079.5:n.405+48C>A
ENST00000394321.9:n.485+48C>A
ENST00000596008.1:n.367+48C>A
ENST00000598406.1:n.226+48C>A
ENST00000601003.1:c.405+48C>A ENSP00000469074.1:n.405+48C>A
NM_020533.2:c.405+48C>A NP_065394.1:n.405+48C>A
NM_020533.3:c.405+48C>A MANE Select NP_065394.1:n.405+48C>A
Search 100 bp 5'
Search 100 bp 3'