Canonical Allele Identifier: CA9585072

Gene: MED25

Linked Data

• dbSNP Id: rs774388864
• ExAC: 19:50333892 C / T
• gnomAD v2: 19-50333892-C-T
• gnomAD v4: 19-49830635-C-T
• MyVariant Identifiers: chr19:g.50333892C>T (hg19) ; chr19:g.49830635C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830635C>T , CM000681.2:g.49830635C>T	GRCh38
NC_000019.9:g.50333892C>T , CM000681.1:g.50333892C>T	GRCh37
NC_000019.8:g.55025704C>T	NCBI36
NG_017091.1:g.17357C>T , LRG_368:g.17357C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.907+37C>T	ENSP00000470692.3:n.907+37C>T
ENST00000312865.10:c.907+37C>T MANE Select	ENSP00000326767.5:n.907+37C>T
ENST00000538643.5:c.268+37C>T	ENSP00000437496.1:n.268+37C>T
ENST00000595185.5:c.688+687C>T	ENSP00000470027.1:n.688+687C>T
ENST00000612791.4:c.761+473C>T	ENSP00000479851.1:n.761+473C>T
ENST00000612854.4:c.450+1620C>T	ENSP00000482155.1:n.450+1620C>T
ENST00000617849.4:c.158-104C>T	ENSP00000484882.1:n.158-104C>T
ENST00000618715.4:c.158-103C>T	ENSP00000480731.1:n.158-103C>T
ENST00000620467.4:c.907+37C>T	ENSP00000482659.1:n.907+37C>T
ENST00000622402.4:c.146-5192C>T	ENSP00000478074.1:n.146-5192C>T
NM_030973.3:c.907+37C>T , LRG_368t1:c.907+37C>T	NP_112235.2:n.907+37C>T
XM_011527353.1:c.907+37C>T	XP_011525655.1:n.907+37C>T
NM_001378355.1:c.907+37C>T	NP_001365284.1:n.907+37C>T
NM_030973.4:c.907+37C>T MANE Select	NP_112235.2:n.907+37C>T