Canonical Allele Identifier: CA2621142339

Gene: MED13L

Linked Data

• gnomAD v4: 12-115984520-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984520A>G , CM000674.2:g.115984520A>G	GRCh38
NC_000012.11:g.116422325A>G , CM000674.1:g.116422325A>G	GRCh37
NC_000012.10:g.114906708A>G	NCBI36
NG_023366.1:g.297667T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4339-148T>C MANE Select	ENSP00000281928.3:n.4339-148T>C
ENST00000549786.2:c.3767-148T>C
ENST00000648379.1:n.2707-148T>C
ENST00000648737.1:n.4103-148T>C
ENST00000648825.1:n.1079-148T>C
ENST00000648916.1:n.2350-148T>C
ENST00000649146.1:n.921T>C
ENST00000649607.1:c.2523-148T>C
ENST00000649775.1:c.836-148T>C
ENST00000650091.1:n.2315-148T>C
ENST00000650226.1:c.4339-148T>C	ENSP00000496981.1:n.4339-148T>C
ENST00000281928.7:c.4339-148T>C	ENSP00000281928.3:n.4339-148T>C
NM_015335.4:c.4339-148T>C	NP_056150.1:n.4339-148T>C
XM_011538080.1:c.4339-148T>C	XP_011536382.1:n.4339-148T>C
XM_011538081.1:c.4336-148T>C	XP_011536383.1:n.4336-148T>C
XM_011538082.1:c.4309-148T>C	XP_011536384.1:n.4309-148T>C
XM_011538080.2:c.4339-148T>C	XP_011536382.1:n.4339-148T>C
XM_011538081.2:c.4336-148T>C	XP_011536383.1:n.4336-148T>C
XM_011538082.2:c.4309-148T>C	XP_011536384.1:n.4309-148T>C
XM_017019090.1:c.4336-148T>C	XP_016874579.1:n.4336-148T>C
NM_015335.5:c.4339-148T>C MANE Select	NP_056150.1:n.4339-148T>C