Canonical Allele Identifier: CA200621938

Gene: MED27

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131939431C>T , CM000671.2:g.131939431C>T	GRCh38
NC_000009.11:g.134814818C>T , CM000671.1:g.134814818C>T	GRCh37
NC_000009.10:g.133804639C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292035.10:c.523G>A MANE Select	ENSP00000292035.5:p.Glu175Lys
ENST00000651555.1:c.523G>A	ENSP00000498641.1:p.Glu175Lys
ENST00000651950.1:c.523G>A	ENSP00000498604.1:p.Glu175Lys
ENST00000292035.9:c.523G>A	ENSP00000292035.5:p.Glu175Lys
ENST00000357028.6:c.523G>A	ENSP00000349530.3:p.Glu175Lys
NM_001253881.1:c.523G>A	NP_001240810.1:p.Glu175Lys
NM_004269.3:c.523G>A	NP_004260.2:p.Glu175Lys
XM_005272236.2:c.523G>A	XP_005272293.1:p.Glu175Lys
XM_005272236.3:c.523G>A	XP_005272293.1:p.Glu175Lys
XM_017015329.1:c.523G>A	XP_016870818.1:p.Glu175Lys
XM_017015330.2:c.523G>A	XP_016870819.1:p.Glu175Lys
NM_004269.4:c.523G>A MANE Select	NP_004260.2:p.Glu175Lys
NM_001253881.2:c.523G>A	NP_001240810.1:p.Glu175Lys