Canonical Allele Identifier: CA481949565

Gene: MED13L

Linked Data

• dbSNP Id: rs1878455941
• MyVariant Identifiers: chr12:g.116434932T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997127T>C , CM000674.2:g.115997127T>C	GRCh38
NC_000012.11:g.116434932T>C , CM000674.1:g.116434932T>C	GRCh37
NC_000012.10:g.114919315T>C	NCBI36
NG_023366.1:g.285060A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2673A>G MANE Select	ENSP00000281928.3:p.Thr891=
ENST00000548743.2:c.2643A>G	ENSP00000448553.2:p.Thr881=
ENST00000549786.2:c.2101A>G
ENST00000647927.1:n.3046A>G
ENST00000648173.1:n.1468A>G
ENST00000648379.1:n.1041A>G
ENST00000648737.1:n.2437A>G
ENST00000648916.1:n.684A>G
ENST00000649607.1:c.857A>G
ENST00000650226.1:c.2673A>G	ENSP00000496981.1:p.Thr891=
ENST00000281928.7:c.2673A>G	ENSP00000281928.3:p.Thr891=
NM_015335.4:c.2673A>G	NP_056150.1:p.Thr891=
XM_011538080.1:c.2673A>G	XP_011536382.1:p.Thr891=
XM_011538081.1:c.2670A>G	XP_011536383.1:p.Thr890=
XM_011538082.1:c.2643A>G	XP_011536384.1:p.Thr881=
XM_011538080.2:c.2673A>G	XP_011536382.1:p.Thr891=
XM_011538081.2:c.2670A>G	XP_011536383.1:p.Thr890=
XM_011538082.2:c.2643A>G	XP_011536384.1:p.Thr881=
XM_017019090.1:c.2670A>G	XP_016874579.1:p.Thr890=
NM_015335.5:c.2673A>G MANE Select	NP_056150.1:p.Thr891=