Canonical Allele Identifier: CA481947938

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116422136T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984331T>G , CM000674.2:g.115984331T>G	GRCh38
NC_000012.11:g.116422136T>G , CM000674.1:g.116422136T>G	GRCh37
NC_000012.10:g.114906519T>G	NCBI36
NG_023366.1:g.297856A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4380A>C MANE Select	ENSP00000281928.3:p.Leu1460=
ENST00000549786.2:c.3808A>C
ENST00000648379.1:n.2748A>C
ENST00000648737.1:n.4144A>C
ENST00000648825.1:n.1120A>C
ENST00000648916.1:n.2391A>C
ENST00000649146.1:n.1110A>C
ENST00000649607.1:c.2564A>C
ENST00000649775.1:c.877A>C
ENST00000650091.1:n.2356A>C
ENST00000650226.1:c.4380A>C	ENSP00000496981.1:p.Leu1460=
ENST00000281928.7:c.4380A>C	ENSP00000281928.3:p.Leu1460=
NM_015335.4:c.4380A>C	NP_056150.1:p.Leu1460=
XM_011538080.1:c.4380A>C	XP_011536382.1:p.Leu1460=
XM_011538081.1:c.4377A>C	XP_011536383.1:p.Leu1459=
XM_011538082.1:c.4350A>C	XP_011536384.1:p.Leu1450=
XM_011538080.2:c.4380A>C	XP_011536382.1:p.Leu1460=
XM_011538081.2:c.4377A>C	XP_011536383.1:p.Leu1459=
XM_011538082.2:c.4350A>C	XP_011536384.1:p.Leu1450=
XM_017019090.1:c.4377A>C	XP_016874579.1:p.Leu1459=
NM_015335.5:c.4380A>C MANE Select	NP_056150.1:p.Leu1460=