Canonical Allele Identifier: CA292044

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49818330A>G , CM000681.2:g.49818330A>G	GRCh38
NC_000019.9:g.50321587A>G , CM000681.1:g.50321587A>G	GRCh37
NC_000019.8:g.55013399A>G	NCBI36
NG_017091.1:g.5052A>G , LRG_368:g.5052A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.-12A>G	ENSP00000470692.3:n.-12A>G
ENST00000312865.10:c.-12A>G MANE Select	ENSP00000326767.5:n.-12A>G
ENST00000593595.1:n.49A>G
ENST00000593636.1:n.42A>G
ENST00000612854.4:c.-12A>G	ENSP00000482155.1:n.-12A>G
ENST00000617849.4:c.-12A>G	ENSP00000484882.1:n.-12A>G
ENST00000620467.4:c.-12A>G	ENSP00000482659.1:n.-12A>G
ENST00000622402.4:c.-12A>G	ENSP00000478074.1:n.-12A>G
NM_030973.3:c.-12A>G , LRG_368t1:c.-12A>G	NP_112235.2:n.-12A>G
XM_011527353.1:c.-12A>G	XP_011525655.1:n.-12A>G
NM_001378355.1:c.-12A>G	NP_001365284.1:n.-12A>G
NM_030973.4:c.-12A>G MANE Select	NP_112235.2:n.-12A>G