Canonical Allele Identifier: CA386883740

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116422123T>G (hg19) ; chr12:g.115984318T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984318T>G , CM000674.2:g.115984318T>G	GRCh38
NC_000012.11:g.116422123T>G , CM000674.1:g.116422123T>G	GRCh37
NC_000012.10:g.114906506T>G	NCBI36
NG_023366.1:g.297869A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4393A>C MANE Select	ENSP00000281928.3:p.Met1465Leu
ENST00000549786.2:c.3821A>C
ENST00000648379.1:n.2761A>C
ENST00000648737.1:n.4157A>C
ENST00000648825.1:n.1133A>C
ENST00000648916.1:n.2404A>C
ENST00000649146.1:n.1123A>C
ENST00000649607.1:c.2577A>C
ENST00000649775.1:c.890A>C
ENST00000650091.1:n.2369A>C
ENST00000650226.1:c.4393A>C	ENSP00000496981.1:p.Met1465Leu
ENST00000281928.7:c.4393A>C	ENSP00000281928.3:p.Met1465Leu
NM_015335.4:c.4393A>C	NP_056150.1:p.Met1465Leu
XM_011538080.1:c.4393A>C	XP_011536382.1:p.Met1465Leu
XM_011538081.1:c.4390A>C	XP_011536383.1:p.Met1464Leu
XM_011538082.1:c.4363A>C	XP_011536384.1:p.Met1455Leu
XM_011538080.2:c.4393A>C	XP_011536382.1:p.Met1465Leu
XM_011538081.2:c.4390A>C	XP_011536383.1:p.Met1464Leu
XM_011538082.2:c.4363A>C	XP_011536384.1:p.Met1455Leu
XM_017019090.1:c.4390A>C	XP_016874579.1:p.Met1464Leu
NM_015335.5:c.4393A>C MANE Select	NP_056150.1:p.Met1465Leu