Canonical Allele Identifier: CA386876208

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116408461G>C (hg19) ; chr12:g.115970656G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970656G>C , CM000674.2:g.115970656G>C	GRCh38
NC_000012.11:g.116408461G>C , CM000674.1:g.116408461G>C	GRCh37
NC_000012.10:g.114892844G>C	NCBI36
NG_023366.1:g.311531C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.6005C>G MANE Select	ENSP00000281928.3:p.Ser2002Ter
ENST00000548784.2:n.2219C>G
ENST00000648379.1:n.4373C>G
ENST00000648737.1:n.5769C>G
ENST00000648825.1:n.4190C>G
ENST00000648916.1:n.4016C>G
ENST00000649607.1:c.4189C>G
ENST00000649775.1:c.2494C>G
ENST00000650226.1:c.6041C>G	ENSP00000496981.1:p.Ser2014Ter
ENST00000281928.7:c.6005C>G	ENSP00000281928.3:p.Ser2002Ter
NM_015335.4:c.6005C>G	NP_056150.1:p.Ser2002Ter
XM_011538080.1:c.6041C>G	XP_011536382.1:p.Ser2014Ter
XM_011538081.1:c.6038C>G	XP_011536383.1:p.Ser2013Ter
XM_011538082.1:c.6011C>G	XP_011536384.1:p.Ser2004Ter
XM_011538080.2:c.6041C>G	XP_011536382.1:p.Ser2014Ter
XM_011538081.2:c.6038C>G	XP_011536383.1:p.Ser2013Ter
XM_011538082.2:c.6011C>G	XP_011536384.1:p.Ser2004Ter
XM_017019090.1:c.6002C>G	XP_016874579.1:p.Ser2001Ter
NM_015335.5:c.6005C>G MANE Select	NP_056150.1:p.Ser2002Ter