Canonical Allele Identifier: CA393769653

Gene: MESP2

Linked Data

• MyVariant Identifiers: chr15:g.90319909T>G (hg19) ; chr15:g.89776678T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89776678T>G , CM000677.2:g.89776678T>G	GRCh38
NC_000015.9:g.90319909T>G , CM000677.1:g.90319909T>G	GRCh37
NC_000015.8:g.88120913T>G	NCBI36
NG_008608.1:g.5321T>G
NG_008608.2:g.21088T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341735.5:c.321T>G MANE Select	ENSP00000342392.3:p.Phe107Leu
ENST00000341735.3:c.321T>G	ENSP00000342392.3:p.Phe107Leu
ENST00000558723.1:n.39-1387T>G
ENST00000560219.2:c.31-1387T>G	ENSP00000452998.1:n.31-1387T>G
NM_001039958.1:c.321T>G	NP_001035047.1:p.Phe107Leu
NM_001039958.2:c.321T>G MANE Select	NP_001035047.1:p.Phe107Leu