Canonical Allele Identifier: CA2065396304

Gene: MED13L

Linked Data

• dbSNP Id: rs1878441068
• gnomAD v4: 12-115996885-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115996885T>C , CM000674.2:g.115996885T>C	GRCh38
NC_000012.11:g.116434690T>C , CM000674.1:g.116434690T>C	GRCh37
NC_000012.10:g.114919073T>C	NCBI36
NG_023366.1:g.285302A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2790+125A>G MANE Select	ENSP00000281928.3:n.2790+125A>G
ENST00000548743.2:c.2760+125A>G	ENSP00000448553.2:n.2760+125A>G
ENST00000549786.2:c.2218+125A>G
ENST00000647927.1:n.3163+125A>G
ENST00000648173.1:n.1585+125A>G
ENST00000648379.1:n.1158+125A>G
ENST00000648737.1:n.2554+125A>G
ENST00000648916.1:n.801+125A>G
ENST00000649607.1:c.974+125A>G
ENST00000650226.1:c.2790+125A>G	ENSP00000496981.1:n.2790+125A>G
ENST00000281928.7:c.2790+125A>G	ENSP00000281928.3:n.2790+125A>G
NM_015335.4:c.2790+125A>G	NP_056150.1:n.2790+125A>G
XM_011538080.1:c.2790+125A>G	XP_011536382.1:n.2790+125A>G
XM_011538081.1:c.2787+125A>G	XP_011536383.1:n.2787+125A>G
XM_011538082.1:c.2760+125A>G	XP_011536384.1:n.2760+125A>G
XM_011538080.2:c.2790+125A>G	XP_011536382.1:n.2790+125A>G
XM_011538081.2:c.2787+125A>G	XP_011536383.1:n.2787+125A>G
XM_011538082.2:c.2760+125A>G	XP_011536384.1:n.2760+125A>G
XM_017019090.1:c.2787+125A>G	XP_016874579.1:n.2787+125A>G
NM_015335.5:c.2790+125A>G MANE Select	NP_056150.1:n.2790+125A>G