Canonical Allele Identifier: CA2586449997

Gene: MED25

Linked Data

• gnomAD v4: 19-49830572-A-ACCAGAAGGCTGGGCTGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830575_49830592dup , CM000681.2:g.49830575_49830592dup	GRCh38
NC_000019.9:g.50333832_50333849dup , CM000681.1:g.50333832_50333849dup	GRCh37
NC_000019.8:g.55025644_55025661dup	NCBI36
NG_017091.1:g.17297_17314dup , LRG_368:g.17297_17314dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.884_901dup	ENSP00000470692.3:p.Gly300_Pro301insGlnLysAlaGlyLeuGly
ENST00000312865.10:c.884_901dup MANE Select	ENSP00000326767.5:p.Gly300_Pro301insGlnLysAlaGlyLeuGly
ENST00000538643.5:c.245_262dup	ENSP00000437496.1:p.Gly87_Pro88insGlnLysAlaGlyLeuGly
ENST00000595185.5:c.688+627_688+644dup	ENSP00000470027.1:n.688+627_688+644dup
ENST00000612791.4:c.761+413_761+430dup	ENSP00000479851.1:n.761+413_761+430dup
ENST00000612854.4:c.450+1560_450+1577dup	ENSP00000482155.1:n.450+1560_450+1577dup
ENST00000617849.4:c.158-164_158-147dup	ENSP00000484882.1:n.158-164_158-147dup
ENST00000618715.4:c.158-163_158-146dup	ENSP00000480731.1:n.158-163_158-146dup
ENST00000620467.4:c.884_901dup	ENSP00000482659.1:p.Gly300_Pro301insGlnLysAlaGlyLeuGly
ENST00000622402.4:c.146-5252_146-5235dup	ENSP00000478074.1:n.146-5252_146-5235dup
NM_030973.3:c.884_901dup , LRG_368t1:c.884_901dup	NP_112235.2:p.Gly300_Pro301insGlnLysAlaGlyLeuGly
XM_011527353.1:c.884_901dup	XP_011525655.1:p.Gly300_Pro301insGlnLysAlaGlyLeuGly
NM_001378355.1:c.884_901dup	NP_001365284.1:p.Gly300_Pro301insGlnLysAlaGlyLeuGly
NM_030973.4:c.884_901dup MANE Select	NP_112235.2:p.Gly300_Pro301insGlnLysAlaGlyLeuGly