Canonical Allele Identifier: CA1321145668

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625863_201625864delinsTG , CM000664.2:g.201625863_201625864delinsTG	GRCh38
NC_000002.11:g.202490586_202490587delinsTG , CM000664.1:g.202490586_202490587delinsTG	GRCh37
NC_000002.10:g.202198831_202198832delinsTG	NCBI36
NG_032049.1:g.22666_22667delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+162_955+163delinsCA
ENST00000621467.5:c.1033+162_1033+163delinsCA	ENSP00000480508.2:n.1033+162_1033+163delinsCA
ENST00000686475.1:n.1099+162_1099+163delinsCA
ENST00000409883.7:c.1159+162_1159+163delinsCA MANE Select	ENSP00000386264.2:n.1159+162_1159+163delinsCA
ENST00000286196.9:c.*723+162_*723+163delinsCA	ENSP00000286196.5:n.*723+162_*723+163delinsCA
ENST00000409444.6:c.1135+162_1135+163delinsCA	ENSP00000387203.2:n.1135+162_1135+163delinsCA
ENST00000409883.6:c.1159+162_1159+163delinsCA	ENSP00000386264.2:n.1159+162_1159+163delinsCA
ENST00000471318.5:n.387+162_387+163delinsCA
ENST00000495329.1:n.298+162_298+163delinsCA
ENST00000621467.4:c.1135+162_1135+163delinsCA	ENSP00000480508.1:n.1135+162_1135+163delinsCA
NM_001044385.2:c.1159+162_1159+163delinsCA	NP_001037850.1:n.1159+162_1159+163delinsCA
NM_152388.3:c.1135+162_1135+163delinsCA	NP_689601.2:n.1135+162_1135+163delinsCA
NM_001044385.3:c.1159+162_1159+163delinsCA MANE Select	NP_001037850.1:n.1159+162_1159+163delinsCA
NM_152388.4:c.1135+162_1135+163delinsCA	NP_689601.2:n.1135+162_1135+163delinsCA