Canonical Allele Identifier: CA1321145897
Gene: TMEM237 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201626057_201626058delinsCA , CM000664.2:g.201626057_201626058delinsCA GRCh38
NC_000002.11:g.202490780_202490781delinsCA , CM000664.1:g.202490780_202490781delinsCA GRCh37
NC_000002.10:g.202199025_202199026delinsCA NCBI36
NG_032049.1:g.22472_22473delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000471318.6:n.923_924delinsTG
ENST00000621467.5:c.1001_1002delinsTG ENSP00000480508.2:p.Leu334=
ENST00000686475.1:n.1067_1068delinsTG
ENST00000409883.7:c.1127_1128delinsTG MANE Select ENSP00000386264.2:p.Leu376=
ENST00000286196.9:c.*691_*692delinsTG ENSP00000286196.5:n.*691_*692delinsTG
ENST00000409444.6:c.1103_1104delinsTG ENSP00000387203.2:p.Leu368=
ENST00000409883.6:c.1127_1128delinsTG ENSP00000386264.2:p.Leu376=
ENST00000471318.5:n.355_356delinsTG
ENST00000495329.1:n.266_267delinsTG
ENST00000621467.4:c.1103_1104delinsTG ENSP00000480508.1:p.Leu368=
NM_001044385.2:c.1127_1128delinsTG NP_001037850.1:p.Leu376=
NM_152388.3:c.1103_1104delinsTG NP_689601.2:p.Leu368=
NM_001044385.3:c.1127_1128delinsTG MANE Select NP_001037850.1:p.Leu376=
NM_152388.4:c.1103_1104delinsTG NP_689601.2:p.Leu368=