Canonical Allele Identifier: CA508141169

Gene: MED25

Linked Data

• MyVariant Identifiers: chr19:g.50334057A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830800A>T , CM000681.2:g.49830800A>T	GRCh38
NC_000019.9:g.50334057A>T , CM000681.1:g.50334057A>T	GRCh37
NC_000019.8:g.55025869A>T	NCBI36
NG_017091.1:g.17522A>T , LRG_368:g.17522A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000593767.3:c.1014A>T	ENSP00000470692.3:p.Pro338=
ENST00000312865.10:c.1014A>T MANE Select	ENSP00000326767.5:p.Pro338=
ENST00000538643.5:c.375A>T	ENSP00000437496.1:p.Pro125=
ENST00000595185.5:c.688+852A>T	ENSP00000470027.1:n.688+852A>T
ENST00000612791.4:c.761+638A>T	ENSP00000479851.1:n.761+638A>T
ENST00000612854.4:c.450+1785A>T	ENSP00000482155.1:n.450+1785A>T
ENST00000617849.4:c.219A>T	ENSP00000484882.1:p.Pro73=
ENST00000618715.4:c.219A>T	ENSP00000480731.1:p.Pro73=
ENST00000620467.4:c.972+42A>T	ENSP00000482659.1:n.972+42A>T
ENST00000622402.4:c.146-5027A>T	ENSP00000478074.1:n.146-5027A>T
NM_030973.3:c.1014A>T , LRG_368t1:c.1014A>T	NP_112235.2:p.Pro338=
XM_011527353.1:c.1014A>T	XP_011525655.1:p.Pro338=
NM_001378355.1:c.1014A>T	NP_001365284.1:p.Pro338=
NM_030973.4:c.1014A>T MANE Select	NP_112235.2:p.Pro338=