Canonical Allele Identifier: CA1149191354
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs1642194370

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535260dup , CM000663.2:g.1535260dup GRCh38
NC_000001.10:g.1470640dup , CM000663.1:g.1470640dup GRCh37
NC_000001.9:g.1460503dup NCBI36
NG_041807.1:g.10103dup
NG_053035.1:g.28118dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*101dup MANE Select ENSP00000368007.4:n.*101dup
ENST00000378733.8:c.*101dup ENSP00000368007.4:n.*101dup
ENST00000425828.1:c.*101dup ENSP00000400311.1:n.*101dup
NM_001114748.1:c.*101dup NP_001108220.1:n.*101dup
NM_001114748.2:c.*101dup MANE Select NP_001108220.1:n.*101dup