Canonical Allele Identifier: CA386876552

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116408540T>C (hg19) ; chr12:g.115970735T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970735T>C , CM000674.2:g.115970735T>C	GRCh38
NC_000012.11:g.116408540T>C , CM000674.1:g.116408540T>C	GRCh37
NC_000012.10:g.114892923T>C	NCBI36
NG_023366.1:g.311452A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5926A>G MANE Select	ENSP00000281928.3:p.Thr1976Ala
ENST00000548784.2:n.2140A>G
ENST00000648379.1:n.4294A>G
ENST00000648737.1:n.5690A>G
ENST00000648825.1:n.4111A>G
ENST00000648916.1:n.3937A>G
ENST00000649607.1:c.4110A>G
ENST00000649775.1:c.2415A>G
ENST00000650226.1:c.5962A>G	ENSP00000496981.1:p.Thr1988Ala
ENST00000281928.7:c.5926A>G	ENSP00000281928.3:p.Thr1976Ala
ENST00000548784.1:n.424A>G
ENST00000552447.1:c.539A>G
NM_015335.4:c.5926A>G	NP_056150.1:p.Thr1976Ala
XM_011538080.1:c.5962A>G	XP_011536382.1:p.Thr1988Ala
XM_011538081.1:c.5959A>G	XP_011536383.1:p.Thr1987Ala
XM_011538082.1:c.5932A>G	XP_011536384.1:p.Thr1978Ala
XM_011538080.2:c.5962A>G	XP_011536382.1:p.Thr1988Ala
XM_011538081.2:c.5959A>G	XP_011536383.1:p.Thr1987Ala
XM_011538082.2:c.5932A>G	XP_011536384.1:p.Thr1978Ala
XM_017019090.1:c.5923A>G	XP_016874579.1:p.Thr1975Ala
NM_015335.5:c.5926A>G MANE Select	NP_056150.1:p.Thr1976Ala