Canonical Allele Identifier: CA244141448

Gene: MED13L

Linked Data

• dbSNP Id: rs1010893033
• gnomAD v3: 12-115982726-G-C
• gnomAD v4: 12-115982726-G-C
• MyVariant Identifiers: chr12:g.116420531G>C (hg19) ; chr12:g.115982726G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982726G>C , CM000674.2:g.115982726G>C	GRCh38
NC_000012.11:g.116420531G>C , CM000674.1:g.116420531G>C	GRCh37
NC_000012.10:g.114904914G>C	NCBI36
NG_023366.1:g.299461C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4956-123C>G MANE Select	ENSP00000281928.3:n.4956-123C>G
ENST00000549786.2:c.4384-123C>G
ENST00000648379.1:n.3324-123C>G
ENST00000648737.1:n.4720-123C>G
ENST00000648825.1:n.1696-123C>G
ENST00000648916.1:n.2967-123C>G
ENST00000649146.1:n.2076C>G
ENST00000649607.1:c.3140-123C>G
ENST00000649775.1:c.1453-131C>G
ENST00000650226.1:c.4956-123C>G	ENSP00000496981.1:n.4956-123C>G
ENST00000281928.7:c.4956-123C>G	ENSP00000281928.3:n.4956-123C>G
ENST00000549786.1:c.320-123C>G
NM_015335.4:c.4956-123C>G	NP_056150.1:n.4956-123C>G
XM_011538080.1:c.4956-123C>G	XP_011536382.1:n.4956-123C>G
XM_011538081.1:c.4953-123C>G	XP_011536383.1:n.4953-123C>G
XM_011538082.1:c.4926-123C>G	XP_011536384.1:n.4926-123C>G
XM_011538080.2:c.4956-123C>G	XP_011536382.1:n.4956-123C>G
XM_011538081.2:c.4953-123C>G	XP_011536383.1:n.4953-123C>G
XM_011538082.2:c.4926-123C>G	XP_011536384.1:n.4926-123C>G
XM_017019090.1:c.4953-123C>G	XP_016874579.1:n.4953-123C>G
NM_015335.5:c.4956-123C>G MANE Select	NP_056150.1:n.4956-123C>G