Canonical Allele Identifier: CA10113886

Gene: MED15

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20583314C>T , CM000684.2:g.20583314C>T	GRCh38
NC_000022.10:g.20937601C>T , CM000684.1:g.20937601C>T	GRCh37
NC_000022.9:g.19267601C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263205.11:c.1673-16C>T MANE Select	ENSP00000263205.7:n.1673-16C>T
ENST00000292733.11:c.1553-16C>T	ENSP00000292733.7:n.1553-16C>T
ENST00000382974.6:c.1340-16C>T	ENSP00000372434.2:n.1340-16C>T
ENST00000406969.5:c.1475-16C>T	ENSP00000384344.1:n.1475-16C>T
ENST00000433831.5:c.*1396-16C>T	ENSP00000391108.1:n.*1396-16C>T
ENST00000473244.5:n.1111-16C>T
ENST00000476187.1:n.174-16C>T
ENST00000489651.5:n.1956-16C>T
ENST00000492381.5:n.2012-16C>T
ENST00000493216.1:n.1155-16C>T
NM_001003891.2:c.1673-16C>T	NP_001003891.1:n.1673-16C>T
NM_001293234.1:c.1502-16C>T	NP_001280163.1:n.1502-16C>T
NM_001293235.1:c.1475-16C>T	NP_001280164.1:n.1475-16C>T
NM_001293236.1:c.1340-16C>T	NP_001280165.1:n.1340-16C>T
NM_001293237.1:c.1475-16C>T	NP_001280166.1:n.1475-16C>T
NM_015889.4:c.1553-16C>T	NP_056973.2:n.1553-16C>T
XM_006724263.2:c.1460-16C>T	XP_006724326.1:n.1460-16C>T
XM_006724264.2:c.1430-16C>T	XP_006724327.1:n.1430-16C>T
XM_011530214.1:c.1595-16C>T	XP_011528516.1:n.1595-16C>T
XM_011530215.1:c.1532-16C>T	XP_011528517.1:n.1532-16C>T
XM_011530216.1:c.1430-16C>T	XP_011528518.1:n.1430-16C>T
XM_011530221.1:c.521-16C>T	XP_011528523.1:n.521-16C>T
XR_002958692.1:n.1770-16C>T
XR_002958693.1:n.1879-16C>T
XR_002958694.1:n.1798-16C>T
XR_002958695.1:n.1650-16C>T
XR_002958696.1:n.1680-16C>T
XR_002958697.1:n.1555-16C>T
XR_002958698.1:n.1781-16C>T
XR_002958699.1:n.1952-16C>T
XR_002958700.1:n.1851-16C>T
XR_002958701.1:n.3061-16C>T
XR_002958702.1:n.1850-16C>T
XR_002958703.1:n.1839-16C>T
NM_001003891.3:c.1673-16C>T MANE Select	NP_001003891.1:n.1673-16C>T
NM_001293234.2:c.1502-16C>T	NP_001280163.1:n.1502-16C>T
NM_001293235.2:c.1475-16C>T	NP_001280164.1:n.1475-16C>T
NM_001293236.2:c.1340-16C>T	NP_001280165.1:n.1340-16C>T
NM_001293237.2:c.1475-16C>T	NP_001280166.1:n.1475-16C>T
NM_015889.5:c.1553-16C>T	NP_056973.2:n.1553-16C>T