Canonical Allele Identifier: CA10113594

Gene: MED15

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20566679G>A , CM000684.2:g.20566679G>A	GRCh38
NC_000022.10:g.20920966G>A , CM000684.1:g.20920966G>A	GRCh37
NC_000022.9:g.19250966G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263205.11:c.903G>A MANE Select	ENSP00000263205.7:p.Pro301=
ENST00000292733.11:c.903G>A	ENSP00000292733.7:p.Pro301=
ENST00000382974.6:c.690G>A	ENSP00000372434.2:p.Pro230=
ENST00000406969.5:c.825G>A	ENSP00000384344.1:p.Pro275=
ENST00000433831.5:c.*746G>A	ENSP00000391108.1:n.*746G>A
ENST00000478831.5:n.215G>A
ENST00000492381.5:n.1362G>A
NM_001003891.2:c.903G>A	NP_001003891.1:p.Pro301=
NM_001293234.1:c.903G>A	NP_001280163.1:p.Pro301=
NM_001293235.1:c.825G>A	NP_001280164.1:p.Pro275=
NM_001293236.1:c.690G>A	NP_001280165.1:p.Pro230=
NM_001293237.1:c.825G>A	NP_001280166.1:p.Pro275=
NM_015889.4:c.903G>A	NP_056973.2:p.Pro301=
XM_006724263.2:c.690G>A	XP_006724326.1:p.Pro230=
XM_006724264.2:c.660G>A	XP_006724327.1:p.Pro220=
XM_011530214.1:c.825G>A	XP_011528516.1:p.Pro275=
XM_011530215.1:c.762G>A	XP_011528517.1:p.Pro254=
XM_011530216.1:c.660G>A	XP_011528518.1:p.Pro220=
XM_011530217.1:c.903G>A	XP_011528519.1:p.Pro301=
XM_011530218.1:c.903G>A	XP_011528520.1:p.Pro301=
XM_011530219.1:c.903G>A	XP_011528521.1:p.Pro301=
XM_011530220.1:c.903G>A	XP_011528522.1:p.Pro301=
XM_011530218.3:c.903G>A	XP_011528520.1:p.Pro301=
XM_011530219.2:c.903G>A	XP_011528521.1:p.Pro301=
XM_011530220.3:c.903G>A	XP_011528522.1:p.Pro301=
XM_017028821.2:c.903G>A	XP_016884310.1:p.Pro301=
XR_002958692.1:n.1000G>A
XR_002958693.1:n.1109G>A
XR_002958694.1:n.1028G>A
XR_002958695.1:n.1000G>A
XR_002958696.1:n.910G>A
XR_002958697.1:n.785G>A
XR_002958698.1:n.1011G>A
XR_002958699.1:n.1182G>A
XR_002958700.1:n.1081G>A
XR_002958701.1:n.963G>A
XR_002958702.1:n.1011G>A
XR_002958703.1:n.1000G>A
NM_001003891.3:c.903G>A MANE Select	NP_001003891.1:p.Pro301=
NM_001293234.2:c.903G>A	NP_001280163.1:p.Pro301=
NM_001293235.2:c.825G>A	NP_001280164.1:p.Pro275=
NM_001293236.2:c.690G>A	NP_001280165.1:p.Pro230=
NM_001293237.2:c.825G>A	NP_001280166.1:p.Pro275=
NM_015889.5:c.903G>A	NP_056973.2:p.Pro301=