Canonical Allele Identifier: CA350304387

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490790C>G (hg19) ; chr2:g.201626067C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626067C>G , CM000664.2:g.201626067C>G	GRCh38
NC_000002.11:g.202490790C>G , CM000664.1:g.202490790C>G	GRCh37
NC_000002.10:g.202199035C>G	NCBI36
NG_032049.1:g.22463G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.914G>C
ENST00000621467.5:c.992G>C	ENSP00000480508.2:p.Trp331Ser
ENST00000686475.1:n.1058G>C
ENST00000409883.7:c.1118G>C MANE Select	ENSP00000386264.2:p.Trp373Ser
ENST00000286196.9:c.*682G>C	ENSP00000286196.5:n.*682G>C
ENST00000409444.6:c.1094G>C	ENSP00000387203.2:p.Trp365Ser
ENST00000409883.6:c.1118G>C	ENSP00000386264.2:p.Trp373Ser
ENST00000471318.5:n.346G>C
ENST00000495329.1:n.257G>C
ENST00000621467.4:c.1094G>C	ENSP00000480508.1:p.Trp365Ser
NM_001044385.2:c.1118G>C	NP_001037850.1:p.Trp373Ser
NM_152388.3:c.1094G>C	NP_689601.2:p.Trp365Ser
NM_001044385.3:c.1118G>C MANE Select	NP_001037850.1:p.Trp373Ser
NM_152388.4:c.1094G>C	NP_689601.2:p.Trp365Ser