Canonical Allele Identifier: CA2587948463
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7527791-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527791C>T , CM000681.2:g.7527791C>T GRCh38
NC_000019.9:g.7592677C>T , CM000681.1:g.7592677C>T GRCh37
NC_000019.8:g.7498677C>T NCBI36
NG_015806.1:g.10182C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.681-73C>T MANE Select ENSP00000264079.5:n.681-73C>T
ENST00000264079.10:c.681-73C>T ENSP00000264079.5:n.681-73C>T
ENST00000394321.9:n.923C>T
ENST00000601003.1:c.572-73C>T ENSP00000469074.1:n.572-73C>T
NM_020533.2:c.681-73C>T NP_065394.1:n.681-73C>T
NM_020533.3:c.681-73C>T MANE Select NP_065394.1:n.681-73C>T