Canonical Allele Identifier: CA2587948289
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7527453-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527453G>T , CM000681.2:g.7527453G>T GRCh38
NC_000019.9:g.7592339G>T , CM000681.1:g.7592339G>T GRCh37
NC_000019.8:g.7498339G>T NCBI36
NG_015806.1:g.9844G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.572-67G>T MANE Select ENSP00000264079.5:n.572-67G>T
ENST00000264079.10:c.572-67G>T ENSP00000264079.5:n.572-67G>T
ENST00000394321.9:n.652-67G>T
ENST00000598406.1:n.393-67G>T
ENST00000601003.1:c.572-411G>T ENSP00000469074.1:n.572-411G>T
NM_020533.2:c.572-67G>T NP_065394.1:n.572-67G>T
NM_020533.3:c.572-67G>T MANE Select NP_065394.1:n.572-67G>T