Canonical Allele Identifier: CA481943164

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116408439T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970634T>G , CM000674.2:g.115970634T>G	GRCh38
NC_000012.11:g.116408439T>G , CM000674.1:g.116408439T>G	GRCh37
NC_000012.10:g.114892822T>G	NCBI36
NG_023366.1:g.311553A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.6027A>C MANE Select	ENSP00000281928.3:p.Pro2009=
ENST00000548784.2:n.2241A>C
ENST00000648379.1:n.4395A>C
ENST00000648737.1:n.5791A>C
ENST00000648825.1:n.4212A>C
ENST00000648916.1:n.4038A>C
ENST00000649607.1:c.4211A>C
ENST00000649775.1:c.2516A>C
ENST00000650226.1:c.6063A>C	ENSP00000496981.1:p.Pro2021=
ENST00000281928.7:c.6027A>C	ENSP00000281928.3:p.Pro2009=
NM_015335.4:c.6027A>C	NP_056150.1:p.Pro2009=
XM_011538080.1:c.6063A>C	XP_011536382.1:p.Pro2021=
XM_011538081.1:c.6060A>C	XP_011536383.1:p.Pro2020=
XM_011538082.1:c.6033A>C	XP_011536384.1:p.Pro2011=
XM_011538080.2:c.6063A>C	XP_011536382.1:p.Pro2021=
XM_011538081.2:c.6060A>C	XP_011536383.1:p.Pro2020=
XM_011538082.2:c.6033A>C	XP_011536384.1:p.Pro2011=
XM_017019090.1:c.6024A>C	XP_016874579.1:p.Pro2008=
NM_015335.5:c.6027A>C MANE Select	NP_056150.1:p.Pro2009=