Canonical Allele Identifier: CA393769657

Gene: MESP2

Linked Data

• MyVariant Identifiers: chr15:g.90319910C>G (hg19) ; chr15:g.89776679C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89776679C>G , CM000677.2:g.89776679C>G	GRCh38
NC_000015.9:g.90319910C>G , CM000677.1:g.90319910C>G	GRCh37
NC_000015.8:g.88120914C>G	NCBI36
NG_008608.1:g.5322C>G
NG_008608.2:g.21089C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000341735.5:c.322C>G MANE Select	ENSP00000342392.3:p.Leu108Val
ENST00000341735.3:c.322C>G	ENSP00000342392.3:p.Leu108Val
ENST00000558723.1:n.39-1386C>G
ENST00000560219.2:c.31-1386C>G	ENSP00000452998.1:n.31-1386C>G
NM_001039958.1:c.322C>G	NP_001035047.1:p.Leu108Val
NM_001039958.2:c.322C>G MANE Select	NP_001035047.1:p.Leu108Val