Canonical Allele Identifier: CA2587950264
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7533402-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533402G>T , CM000681.2:g.7533402G>T GRCh38
NC_000019.9:g.7598288G>T , CM000681.1:g.7598288G>T GRCh37
NC_000019.8:g.7504288G>T NCBI36
NG_013374.1:g.4251G>T
NG_015806.1:g.15793G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1576-121G>T MANE Select ENSP00000264079.5:n.1576-121G>T
ENST00000264079.10:c.1576-121G>T ENSP00000264079.5:n.1576-121G>T
ENST00000394321.9:n.1891-121G>T
ENST00000599334.1:c.304-121G>T
ENST00000602227.1:n.9G>T
NM_020533.2:c.1576-121G>T NP_065394.1:n.1576-121G>T
NM_020533.3:c.1576-121G>T MANE Select NP_065394.1:n.1576-121G>T