Canonical Allele Identifier: CA386876127

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116408424A>T (hg19) ; chr12:g.115970619A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970619A>T , CM000674.2:g.115970619A>T	GRCh38
NC_000012.11:g.116408424A>T , CM000674.1:g.116408424A>T	GRCh37
NC_000012.10:g.114892807A>T	NCBI36
NG_023366.1:g.311568T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.6042T>A MANE Select	ENSP00000281928.3:p.Asn2014Lys
ENST00000548784.2:n.2256T>A
ENST00000648379.1:n.4410T>A
ENST00000648737.1:n.5806T>A
ENST00000648825.1:n.4227T>A
ENST00000648916.1:n.4053T>A
ENST00000649607.1:c.4226T>A
ENST00000649775.1:c.2531T>A
ENST00000650226.1:c.6078T>A	ENSP00000496981.1:p.Asn2026Lys
ENST00000281928.7:c.6042T>A	ENSP00000281928.3:p.Asn2014Lys
NM_015335.4:c.6042T>A	NP_056150.1:p.Asn2014Lys
XM_011538080.1:c.6078T>A	XP_011536382.1:p.Asn2026Lys
XM_011538081.1:c.6075T>A	XP_011536383.1:p.Asn2025Lys
XM_011538082.1:c.6048T>A	XP_011536384.1:p.Asn2016Lys
XM_011538080.2:c.6078T>A	XP_011536382.1:p.Asn2026Lys
XM_011538081.2:c.6075T>A	XP_011536383.1:p.Asn2025Lys
XM_011538082.2:c.6048T>A	XP_011536384.1:p.Asn2016Lys
XM_017019090.1:c.6039T>A	XP_016874579.1:p.Asn2013Lys
NM_015335.5:c.6042T>A MANE Select	NP_056150.1:p.Asn2014Lys