Canonical Allele Identifier: CA386878493

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116413070T>G (hg19) ; chr12:g.115975265T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115975265T>G , CM000674.2:g.115975265T>G	GRCh38
NC_000012.11:g.116413070T>G , CM000674.1:g.116413070T>G	GRCh37
NC_000012.10:g.114897453T>G	NCBI36
NG_023366.1:g.306922A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5637A>C MANE Select	ENSP00000281928.3:p.Leu1879Phe
ENST00000548694.2:n.627A>C
ENST00000648379.1:n.4005A>C
ENST00000648737.1:n.5401A>C
ENST00000648825.1:n.3822A>C
ENST00000648916.1:n.3648A>C
ENST00000649607.1:c.3821A>C
ENST00000649775.1:c.2126A>C
ENST00000650226.1:c.5673A>C	ENSP00000496981.1:p.Leu1891Phe
ENST00000281928.7:c.5637A>C	ENSP00000281928.3:p.Leu1879Phe
ENST00000548694.1:n.627A>C
ENST00000552447.1:c.250A>C
NM_015335.4:c.5637A>C	NP_056150.1:p.Leu1879Phe
XM_011538080.1:c.5673A>C	XP_011536382.1:p.Leu1891Phe
XM_011538081.1:c.5670A>C	XP_011536383.1:p.Leu1890Phe
XM_011538082.1:c.5643A>C	XP_011536384.1:p.Leu1881Phe
XM_011538080.2:c.5673A>C	XP_011536382.1:p.Leu1891Phe
XM_011538081.2:c.5670A>C	XP_011536383.1:p.Leu1890Phe
XM_011538082.2:c.5643A>C	XP_011536384.1:p.Leu1881Phe
XM_017019090.1:c.5634A>C	XP_016874579.1:p.Leu1878Phe
NM_015335.5:c.5637A>C MANE Select	NP_056150.1:p.Leu1879Phe