Canonical Allele Identifier: CA386876130

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116408425T>G (hg19) ; chr12:g.115970620T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970620T>G , CM000674.2:g.115970620T>G	GRCh38
NC_000012.11:g.116408425T>G , CM000674.1:g.116408425T>G	GRCh37
NC_000012.10:g.114892808T>G	NCBI36
NG_023366.1:g.311567A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.6041A>C MANE Select	ENSP00000281928.3:p.Asn2014Thr
ENST00000548784.2:n.2255A>C
ENST00000648379.1:n.4409A>C
ENST00000648737.1:n.5805A>C
ENST00000648825.1:n.4226A>C
ENST00000648916.1:n.4052A>C
ENST00000649607.1:c.4225A>C
ENST00000649775.1:c.2530A>C
ENST00000650226.1:c.6077A>C	ENSP00000496981.1:p.Asn2026Thr
ENST00000281928.7:c.6041A>C	ENSP00000281928.3:p.Asn2014Thr
NM_015335.4:c.6041A>C	NP_056150.1:p.Asn2014Thr
XM_011538080.1:c.6077A>C	XP_011536382.1:p.Asn2026Thr
XM_011538081.1:c.6074A>C	XP_011536383.1:p.Asn2025Thr
XM_011538082.1:c.6047A>C	XP_011536384.1:p.Asn2016Thr
XM_011538080.2:c.6077A>C	XP_011536382.1:p.Asn2026Thr
XM_011538081.2:c.6074A>C	XP_011536383.1:p.Asn2025Thr
XM_011538082.2:c.6047A>C	XP_011536384.1:p.Asn2016Thr
XM_017019090.1:c.6038A>C	XP_016874579.1:p.Asn2013Thr
NM_015335.5:c.6041A>C MANE Select	NP_056150.1:p.Asn2014Thr