Canonical Allele Identifier: CA2065410917

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970710_115970712delinsTGA , CM000674.2:g.115970710_115970712delinsTGA	GRCh38
NC_000012.11:g.116408515_116408517delinsTGA , CM000674.1:g.116408515_116408517delinsTGA	GRCh37
NC_000012.10:g.114892898_114892900delinsTGA	NCBI36
NG_023366.1:g.311475_311477delinsTCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.5949_5951delinsTCA MANE Select	ENSP00000281928.3:p.Ser1983=
ENST00000548784.2:n.2163_2165delinsTCA
ENST00000648379.1:n.4317_4319delinsTCA
ENST00000648737.1:n.5713_5715delinsTCA
ENST00000648825.1:n.4134_4136delinsTCA
ENST00000648916.1:n.3960_3962delinsTCA
ENST00000649607.1:c.4133_4135delinsTCA
ENST00000649775.1:c.2438_2440delinsTCA
ENST00000650226.1:c.5985_5987delinsTCA	ENSP00000496981.1:p.Ser1995=
ENST00000281928.7:c.5949_5951delinsTCA	ENSP00000281928.3:p.Ser1983=
ENST00000548784.1:n.447_449delinsTCA
ENST00000552447.1:c.562_564delinsTCA
NM_015335.4:c.5949_5951delinsTCA	NP_056150.1:p.Ser1983=
XM_011538080.1:c.5985_5987delinsTCA	XP_011536382.1:p.Ser1995=
XM_011538081.1:c.5982_5984delinsTCA	XP_011536383.1:p.Ser1994=
XM_011538082.1:c.5955_5957delinsTCA	XP_011536384.1:p.Ser1985=
XM_011538080.2:c.5985_5987delinsTCA	XP_011536382.1:p.Ser1995=
XM_011538081.2:c.5982_5984delinsTCA	XP_011536383.1:p.Ser1994=
XM_011538082.2:c.5955_5957delinsTCA	XP_011536384.1:p.Ser1985=
XM_017019090.1:c.5946_5948delinsTCA	XP_016874579.1:p.Ser1982=
NM_015335.5:c.5949_5951delinsTCA MANE Select	NP_056150.1:p.Ser1983=