Canonical Allele Identifier: CA2841535875

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970553dup , CM000674.2:g.115970553dup	GRCh38
NC_000012.11:g.116408358dup , CM000674.1:g.116408358dup	GRCh37
NC_000012.10:g.114892741dup	NCBI36
NG_023366.1:g.311634dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.6067+41dup MANE Select	ENSP00000281928.3:n.6067+41dup
ENST00000548784.2:n.2281+41dup
ENST00000648379.1:n.4435+41dup
ENST00000648737.1:n.5831+41dup
ENST00000648825.1:n.4252+41dup
ENST00000648916.1:n.4078+41dup
ENST00000649607.1:c.4251+41dup
ENST00000649775.1:c.2556+41dup
ENST00000650226.1:c.6103+41dup	ENSP00000496981.1:n.6103+41dup
ENST00000281928.7:c.6067+41dup	ENSP00000281928.3:n.6067+41dup
NM_015335.4:c.6067+41dup	NP_056150.1:n.6067+41dup
XM_011538080.1:c.6103+41dup	XP_011536382.1:n.6103+41dup
XM_011538081.1:c.6100+41dup	XP_011536383.1:n.6100+41dup
XM_011538082.1:c.6073+41dup	XP_011536384.1:n.6073+41dup
XM_011538080.2:c.6103+41dup	XP_011536382.1:n.6103+41dup
XM_011538081.2:c.6100+41dup	XP_011536383.1:n.6100+41dup
XM_011538082.2:c.6073+41dup	XP_011536384.1:n.6073+41dup
XM_017019090.1:c.6064+41dup	XP_016874579.1:n.6064+41dup
NM_015335.5:c.6067+41dup MANE Select	NP_056150.1:n.6067+41dup