Canonical Allele Identifier: CA2587949510
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530188_7530221del , CM000681.2:g.7530188_7530221del GRCh38
NC_000019.9:g.7595074_7595107del , CM000681.1:g.7595074_7595107del GRCh37
NC_000019.8:g.7501074_7501107del NCBI36
NG_013374.1:g.1037_1070del
NG_015806.1:g.12579_12612del

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-98_1360-65del MANE Select ENSP00000264079.5:n.1360-98_1360-65del
ENST00000264079.10:c.1360-98_1360-65del ENSP00000264079.5:n.1360-98_1360-65del
ENST00000394321.9:n.1675-98_1675-65del
ENST00000594692.1:n.356-98_356-65del
ENST00000595860.5:n.543-98_543-65del
ENST00000599334.1:c.237-247_237-214del
NM_020533.2:c.1360-98_1360-65del NP_065394.1:n.1360-98_1360-65del
NM_020533.3:c.1360-98_1360-65del MANE Select NP_065394.1:n.1360-98_1360-65del