Canonical Allele Identifier: CA2577211811
Gene: TMEM237 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201625977A>G , CM000664.2:g.201625977A>G GRCh38
NC_000002.11:g.202490700A>G , CM000664.1:g.202490700A>G GRCh37
NC_000002.10:g.202198945A>G NCBI36
NG_032049.1:g.22553T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000471318.6:n.955+49T>C
ENST00000621467.5:c.1033+49T>C ENSP00000480508.2:n.1033+49T>C
ENST00000686475.1:n.1099+49T>C
ENST00000409883.7:c.1159+49T>C MANE Select ENSP00000386264.2:n.1159+49T>C
ENST00000286196.9:c.*723+49T>C ENSP00000286196.5:n.*723+49T>C
ENST00000409444.6:c.1135+49T>C ENSP00000387203.2:n.1135+49T>C
ENST00000409883.6:c.1159+49T>C ENSP00000386264.2:n.1159+49T>C
ENST00000471318.5:n.387+49T>C
ENST00000495329.1:n.298+49T>C
ENST00000621467.4:c.1135+49T>C ENSP00000480508.1:n.1135+49T>C
NM_001044385.2:c.1159+49T>C NP_001037850.1:n.1159+49T>C
NM_152388.3:c.1135+49T>C NP_689601.2:n.1135+49T>C
NM_001044385.3:c.1159+49T>C MANE Select NP_001037850.1:n.1159+49T>C
NM_152388.4:c.1135+49T>C NP_689601.2:n.1135+49T>C
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