Canonical Allele Identifier: CA2575306508

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982633A>G , CM000674.2:g.115982633A>G	GRCh38
NC_000012.11:g.116420438A>G , CM000674.1:g.116420438A>G	GRCh37
NC_000012.10:g.114904821A>G	NCBI36
NG_023366.1:g.299554T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4956-30T>C MANE Select	ENSP00000281928.3:n.4956-30T>C
ENST00000549786.2:c.4384-30T>C
ENST00000648379.1:n.3324-30T>C
ENST00000648737.1:n.4720-30T>C
ENST00000648825.1:n.1696-30T>C
ENST00000648916.1:n.2967-30T>C
ENST00000649146.1:n.2169T>C
ENST00000649607.1:c.3140-30T>C
ENST00000649775.1:c.1453-38T>C
ENST00000650226.1:c.4956-30T>C	ENSP00000496981.1:n.4956-30T>C
ENST00000281928.7:c.4956-30T>C	ENSP00000281928.3:n.4956-30T>C
ENST00000549786.1:c.320-30T>C
NM_015335.4:c.4956-30T>C	NP_056150.1:n.4956-30T>C
XM_011538080.1:c.4956-30T>C	XP_011536382.1:n.4956-30T>C
XM_011538081.1:c.4953-30T>C	XP_011536383.1:n.4953-30T>C
XM_011538082.1:c.4926-30T>C	XP_011536384.1:n.4926-30T>C
XM_011538080.2:c.4956-30T>C	XP_011536382.1:n.4956-30T>C
XM_011538081.2:c.4953-30T>C	XP_011536383.1:n.4953-30T>C
XM_011538082.2:c.4926-30T>C	XP_011536384.1:n.4926-30T>C
XM_017019090.1:c.4953-30T>C	XP_016874579.1:n.4953-30T>C
NM_015335.5:c.4956-30T>C MANE Select	NP_056150.1:n.4956-30T>C