Canonical Allele Identifier: CA415768636
Gene: TMEM240 HGNC NCBI

Linked Data

gnomAD v4: 1-1535666-CA-C
MyVariant Identifiers: chr1:g.1471047del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535670del , CM000663.2:g.1535670del GRCh38
NC_000001.10:g.1471050del , CM000663.1:g.1471050del GRCh37
NC_000001.9:g.1460913del NCBI36
NG_041807.1:g.9694del
NG_053035.1:g.28528del

Transcript Alleles

HGVS Amino-acid change
ENST00000378733.9:c.295del MANE Select ENSP00000368007.4:p.Cys99AlafsTer?
ENST00000378733.8:c.295del ENSP00000368007.4:p.Cys99AlafsTer?
ENST00000425828.1:c.295del ENSP00000400311.1:p.Cys99AlafsTer?
NM_001114748.1:c.295del NP_001108220.1:p.Cys99AlafsTer?
NM_001114748.2:c.295del MANE Select NP_001108220.1:p.Cys99AlafsTer?