Canonical Allele Identifier: CA492295443

Gene: MESP2

Linked Data

• gnomAD v4: 15-89776876-G-T
• MyVariant Identifiers: chr15:g.90320107G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89776876G>T , CM000677.2:g.89776876G>T	GRCh38
NC_000015.9:g.90320107G>T , CM000677.1:g.90320107G>T	GRCh37
NC_000015.8:g.88121111G>T	NCBI36
NG_008608.1:g.5519G>T
NG_008608.2:g.21286G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000341735.5:c.519G>T MANE Select	ENSP00000342392.3:p.Ala173=
ENST00000341735.3:c.519G>T	ENSP00000342392.3:p.Ala173=
ENST00000558723.1:n.39-1189G>T
ENST00000560219.2:c.31-1189G>T	ENSP00000452998.1:n.31-1189G>T
NM_001039958.1:c.519G>T	NP_001035047.1:p.Ala173=
NM_001039958.2:c.519G>T MANE Select	NP_001035047.1:p.Ala173=