Canonical Allele Identifier: CA393770322

Gene: MESP2

Linked Data

• gnomAD v4: 15-89776810-G-T
• MyVariant Identifiers: chr15:g.90320041G>T (hg19) ; chr15:g.89776810G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89776810G>T , CM000677.2:g.89776810G>T	GRCh38
NC_000015.9:g.90320041G>T , CM000677.1:g.90320041G>T	GRCh37
NC_000015.8:g.88121045G>T	NCBI36
NG_008608.1:g.5453G>T
NG_008608.2:g.21220G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341735.5:c.453G>T MANE Select	ENSP00000342392.3:p.Arg151Ser
ENST00000341735.3:c.453G>T	ENSP00000342392.3:p.Arg151Ser
ENST00000558723.1:n.39-1255G>T
ENST00000560219.2:c.31-1255G>T	ENSP00000452998.1:n.31-1255G>T
NM_001039958.1:c.453G>T	NP_001035047.1:p.Arg151Ser
NM_001039958.2:c.453G>T MANE Select	NP_001035047.1:p.Arg151Ser