Canonical Allele Identifier: CA2753880762

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623462_201623463insAAAAAAAAA , CM000664.2:g.201623462_201623463insAAAAAAAAA	GRCh38
NC_000002.11:g.202488185_202488186insAAAAAAAAA , CM000664.1:g.202488185_202488186insAAAAAAAAA	GRCh37
NC_000002.10:g.202196430_202196431insAAAAAAAAA	NCBI36
NG_032049.1:g.25068_25069insTTTTTTTTT
NG_051007.1:g.721_722insTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*793_*794insTTTTTTTTT	ENSP00000480508.2:n.*793_*794insTTTTTTTTT
ENST00000686475.1:n.1960_1961insTTTTTTTTT
ENST00000409883.7:c.*793_*794insTTTTTTTTT MANE Select	ENSP00000386264.2:n.*793_*794insTTTTTTTTT
ENST00000409444.6:c.*793_*794insTTTTTTTTT	ENSP00000387203.2:n.*793_*794insTTTTTTTTT
ENST00000409883.6:c.*793_*794insTTTTTTTTT	ENSP00000386264.2:n.*793_*794insTTTTTTTTT
ENST00000495329.1:n.1159_1160insTTTTTTTTT
NM_001044385.2:c.*793_*794insTTTTTTTTT	NP_001037850.1:n.*793_*794insTTTTTTTTT
NM_152388.3:c.*793_*794insTTTTTTTTT	NP_689601.2:n.*793_*794insTTTTTTTTT
NM_001044385.3:c.*793_*794insTTTTTTTTT MANE Select	NP_001037850.1:n.*793_*794insTTTTTTTTT
NM_152388.4:c.*793_*794insTTTTTTTTT	NP_689601.2:n.*793_*794insTTTTTTTTT