Canonical Allele Identifier: CA2065410899

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970661_115970662delinsTG , CM000674.2:g.115970661_115970662delinsTG	GRCh38
NC_000012.11:g.116408466_116408467delinsTG , CM000674.1:g.116408466_116408467delinsTG	GRCh37
NC_000012.10:g.114892849_114892850delinsTG	NCBI36
NG_023366.1:g.311525_311526delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5999_6000delinsCA MANE Select	ENSP00000281928.3:p.Pro2000=
ENST00000548784.2:n.2213_2214delinsCA
ENST00000648379.1:n.4367_4368delinsCA
ENST00000648737.1:n.5763_5764delinsCA
ENST00000648825.1:n.4184_4185delinsCA
ENST00000648916.1:n.4010_4011delinsCA
ENST00000649607.1:c.4183_4184delinsCA
ENST00000649775.1:c.2488_2489delinsCA
ENST00000650226.1:c.6035_6036delinsCA	ENSP00000496981.1:p.Pro2012=
ENST00000281928.7:c.5999_6000delinsCA	ENSP00000281928.3:p.Pro2000=
NM_015335.4:c.5999_6000delinsCA	NP_056150.1:p.Pro2000=
XM_011538080.1:c.6035_6036delinsCA	XP_011536382.1:p.Pro2012=
XM_011538081.1:c.6032_6033delinsCA	XP_011536383.1:p.Pro2011=
XM_011538082.1:c.6005_6006delinsCA	XP_011536384.1:p.Pro2002=
XM_011538080.2:c.6035_6036delinsCA	XP_011536382.1:p.Pro2012=
XM_011538081.2:c.6032_6033delinsCA	XP_011536383.1:p.Pro2011=
XM_011538082.2:c.6005_6006delinsCA	XP_011536384.1:p.Pro2002=
XM_017019090.1:c.5996_5997delinsCA	XP_016874579.1:p.Pro1999=
NM_015335.5:c.5999_6000delinsCA MANE Select	NP_056150.1:p.Pro2000=