Canonical Allele Identifier: CA633659114

Gene: MED25

Linked Data

• dbSNP Id: rs1415655660
• gnomAD v2: 19-50333878-A-AGG
• gnomAD v4: 19-49830621-A-AGG
• MyVariant Identifiers: chr19:g.50333878_50333879insGG (hg19) ; chr19:g.49830621_49830622insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830623_49830624dup , CM000681.2:g.49830623_49830624dup	GRCh38
NC_000019.9:g.50333880_50333881dup , CM000681.1:g.50333880_50333881dup	GRCh37
NC_000019.8:g.55025692_55025693dup	NCBI36
NG_017091.1:g.17345_17346dup , LRG_368:g.17345_17346dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.907+25_907+26dup	ENSP00000470692.3:n.907+25_907+26dup
ENST00000312865.10:c.907+25_907+26dup MANE Select	ENSP00000326767.5:n.907+25_907+26dup
ENST00000538643.5:c.268+25_268+26dup	ENSP00000437496.1:n.268+25_268+26dup
ENST00000595185.5:c.688+675_688+676dup	ENSP00000470027.1:n.688+675_688+676dup
ENST00000612791.4:c.761+461_761+462dup	ENSP00000479851.1:n.761+461_761+462dup
ENST00000612854.4:c.450+1608_450+1609dup	ENSP00000482155.1:n.450+1608_450+1609dup
ENST00000617849.4:c.158-116_158-115dup	ENSP00000484882.1:n.158-116_158-115dup
ENST00000618715.4:c.158-115_158-114dup	ENSP00000480731.1:n.158-115_158-114dup
ENST00000620467.4:c.907+25_907+26dup	ENSP00000482659.1:n.907+25_907+26dup
ENST00000622402.4:c.146-5204_146-5203dup	ENSP00000478074.1:n.146-5204_146-5203dup
NM_030973.3:c.907+25_907+26dup , LRG_368t1:c.907+25_907+26dup	NP_112235.2:n.907+25_907+26dup
XM_011527353.1:c.907+25_907+26dup	XP_011525655.1:n.907+25_907+26dup
NM_001378355.1:c.907+25_907+26dup	NP_001365284.1:n.907+25_907+26dup
NM_030973.4:c.907+25_907+26dup MANE Select	NP_112235.2:n.907+25_907+26dup