Canonical Allele Identifier: CA2065412955

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975355_115975356delinsTA , CM000674.2:g.115975355_115975356delinsTA	GRCh38
NC_000012.11:g.116413160_116413161delinsTA , CM000674.1:g.116413160_116413161delinsTA	GRCh37
NC_000012.10:g.114897543_114897544delinsTA	NCBI36
NG_023366.1:g.306831_306832delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5589-43_5589-42delinsTA MANE Select	ENSP00000281928.3:n.5589-43_5589-42delinsTA
ENST00000548694.2:n.536_537delinsTA
ENST00000648379.1:n.3957-43_3957-42delinsTA
ENST00000648737.1:n.5353-43_5353-42delinsTA
ENST00000648825.1:n.3774-43_3774-42delinsTA
ENST00000648916.1:n.3600-43_3600-42delinsTA
ENST00000649607.1:c.3773-43_3773-42delinsTA
ENST00000649775.1:c.2078-43_2078-42delinsTA
ENST00000650226.1:c.5589-7_5589-6delinsTA	ENSP00000496981.1:n.5589-7_5589-6delinsTA
ENST00000281928.7:c.5589-43_5589-42delinsTA	ENSP00000281928.3:n.5589-43_5589-42delinsTA
ENST00000548694.1:n.536_537delinsTA
ENST00000552447.1:c.166-7_166-6delinsTA
NM_015335.4:c.5589-43_5589-42delinsTA	NP_056150.1:n.5589-43_5589-42delinsTA
XM_011538080.1:c.5589-7_5589-6delinsTA	XP_011536382.1:n.5589-7_5589-6delinsTA
XM_011538081.1:c.5586-7_5586-6delinsTA	XP_011536383.1:n.5586-7_5586-6delinsTA
XM_011538082.1:c.5559-7_5559-6delinsTA	XP_011536384.1:n.5559-7_5559-6delinsTA
XM_011538080.2:c.5589-7_5589-6delinsTA	XP_011536382.1:n.5589-7_5589-6delinsTA
XM_011538081.2:c.5586-7_5586-6delinsTA	XP_011536383.1:n.5586-7_5586-6delinsTA
XM_011538082.2:c.5559-7_5559-6delinsTA	XP_011536384.1:n.5559-7_5559-6delinsTA
XM_017019090.1:c.5586-43_5586-42delinsTA	XP_016874579.1:n.5586-43_5586-42delinsTA
NM_015335.5:c.5589-43_5589-42delinsTA MANE Select	NP_056150.1:n.5589-43_5589-42delinsTA