Canonical Allele Identifier: CA406914629

Gene: MED25

Linked Data

• MyVariant Identifiers: chr19:g.50333833G>C (hg19) ; chr19:g.49830576G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830576G>C , CM000681.2:g.49830576G>C	GRCh38
NC_000019.9:g.50333833G>C , CM000681.1:g.50333833G>C	GRCh37
NC_000019.8:g.55025645G>C	NCBI36
NG_017091.1:g.17298G>C , LRG_368:g.17298G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.885G>C	ENSP00000470692.3:p.Gln295His
ENST00000312865.10:c.885G>C MANE Select	ENSP00000326767.5:p.Gln295His
ENST00000538643.5:c.246G>C	ENSP00000437496.1:p.Gln82His
ENST00000595185.5:c.688+628G>C	ENSP00000470027.1:n.688+628G>C
ENST00000612791.4:c.761+414G>C	ENSP00000479851.1:n.761+414G>C
ENST00000612854.4:c.450+1561G>C	ENSP00000482155.1:n.450+1561G>C
ENST00000617849.4:c.158-163G>C	ENSP00000484882.1:n.158-163G>C
ENST00000618715.4:c.158-162G>C	ENSP00000480731.1:n.158-162G>C
ENST00000620467.4:c.885G>C	ENSP00000482659.1:p.Gln295His
ENST00000622402.4:c.146-5251G>C	ENSP00000478074.1:n.146-5251G>C
NM_030973.3:c.885G>C , LRG_368t1:c.885G>C	NP_112235.2:p.Gln295His
XM_011527353.1:c.885G>C	XP_011525655.1:p.Gln295His
NM_001378355.1:c.885G>C	NP_001365284.1:p.Gln295His
NM_030973.4:c.885G>C MANE Select	NP_112235.2:p.Gln295His