Canonical Allele Identifier: CA1321145713

Gene: TMEM237

Linked Data

• dbSNP Id: rs1957754409

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625913_201625918dup , CM000664.2:g.201625913_201625918dup	GRCh38
NC_000002.11:g.202490636_202490641dup , CM000664.1:g.202490636_202490641dup	GRCh37
NC_000002.10:g.202198881_202198886dup	NCBI36
NG_032049.1:g.22615_22620dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000471318.6:n.955+111_955+116dup
ENST00000621467.5:c.1033+111_1033+116dup	ENSP00000480508.2:n.1033+111_1033+116dup
ENST00000686475.1:n.1099+111_1099+116dup
ENST00000409883.7:c.1159+111_1159+116dup MANE Select	ENSP00000386264.2:n.1159+111_1159+116dup
ENST00000286196.9:c.*723+111_*723+116dup	ENSP00000286196.5:n.*723+111_*723+116dup
ENST00000409444.6:c.1135+111_1135+116dup	ENSP00000387203.2:n.1135+111_1135+116dup
ENST00000409883.6:c.1159+111_1159+116dup	ENSP00000386264.2:n.1159+111_1159+116dup
ENST00000471318.5:n.387+111_387+116dup
ENST00000495329.1:n.298+111_298+116dup
ENST00000621467.4:c.1135+111_1135+116dup	ENSP00000480508.1:n.1135+111_1135+116dup
NM_001044385.2:c.1159+111_1159+116dup	NP_001037850.1:n.1159+111_1159+116dup
NM_152388.3:c.1135+111_1135+116dup	NP_689601.2:n.1135+111_1135+116dup
NM_001044385.3:c.1159+111_1159+116dup MANE Select	NP_001037850.1:n.1159+111_1159+116dup
NM_152388.4:c.1135+111_1135+116dup	NP_689601.2:n.1135+111_1135+116dup