Canonical Allele Identifier: CA415768642
Gene: TMEM240 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1471056G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535676G>A , CM000663.2:g.1535676G>A GRCh38
NC_000001.10:g.1471056G>A , CM000663.1:g.1471056G>A GRCh37
NC_000001.9:g.1460919G>A NCBI36
NG_041807.1:g.9685C>T
NG_053035.1:g.28534G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378733.9:c.286C>T MANE Select ENSP00000368007.4:p.Leu96=
ENST00000378733.8:c.286C>T ENSP00000368007.4:p.Leu96=
ENST00000425828.1:c.286C>T ENSP00000400311.1:p.Leu96=
NM_001114748.1:c.286C>T NP_001108220.1:p.Leu96=
NM_001114748.2:c.286C>T MANE Select NP_001108220.1:p.Leu96=