Canonical Allele Identifier: CA2587950166
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7533302-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533302A>T , CM000681.2:g.7533302A>T GRCh38
NC_000019.9:g.7598188A>T , CM000681.1:g.7598188A>T GRCh37
NC_000019.8:g.7504188A>T NCBI36
NG_013374.1:g.4151A>T
NG_015806.1:g.15693A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1576-221A>T MANE Select ENSP00000264079.5:n.1576-221A>T
ENST00000264079.10:c.1576-221A>T ENSP00000264079.5:n.1576-221A>T
ENST00000394321.9:n.1891-221A>T
ENST00000599334.1:c.304-221A>T
NM_020533.2:c.1576-221A>T NP_065394.1:n.1576-221A>T
NM_020533.3:c.1576-221A>T MANE Select NP_065394.1:n.1576-221A>T