Canonical Allele Identifier: CA403091491
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533568A>C , CM000681.2:g.7533568A>C GRCh38
NC_000019.9:g.7598454A>C , CM000681.1:g.7598454A>C GRCh37
NC_000019.8:g.7504454A>C NCBI36
NG_013374.1:g.4417A>C
NG_015806.1:g.15959A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1621A>C MANE Select ENSP00000264079.5:p.Ile541Leu
ENST00000264079.10:c.1621A>C ENSP00000264079.5:p.Ile541Leu
ENST00000394321.9:n.1936A>C
ENST00000599334.1:c.349A>C
ENST00000602227.1:n.175A>C
NM_020533.2:c.1621A>C NP_065394.1:p.Ile541Leu
NM_020533.3:c.1621A>C MANE Select NP_065394.1:p.Ile541Leu