Canonical Allele Identifier: CA607651451

Gene: MED13L

Linked Data

• dbSNP Id: rs1243888845
• gnomAD v2: 12-116420460-A-G
• gnomAD v3: 12-115982655-A-G
• gnomAD v4: 12-115982655-A-G
• MyVariant Identifiers: chr12:g.116420460A>G (hg19) ; chr12:g.115982655A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982655A>G , CM000674.2:g.115982655A>G	GRCh38
NC_000012.11:g.116420460A>G , CM000674.1:g.116420460A>G	GRCh37
NC_000012.10:g.114904843A>G	NCBI36
NG_023366.1:g.299532T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4956-52T>C MANE Select	ENSP00000281928.3:n.4956-52T>C
ENST00000549786.2:c.4384-52T>C
ENST00000648379.1:n.3324-52T>C
ENST00000648737.1:n.4720-52T>C
ENST00000648825.1:n.1696-52T>C
ENST00000648916.1:n.2967-52T>C
ENST00000649146.1:n.2147T>C
ENST00000649607.1:c.3140-52T>C
ENST00000649775.1:c.1453-60T>C
ENST00000650226.1:c.4956-52T>C	ENSP00000496981.1:n.4956-52T>C
ENST00000281928.7:c.4956-52T>C	ENSP00000281928.3:n.4956-52T>C
ENST00000549786.1:c.320-52T>C
NM_015335.4:c.4956-52T>C	NP_056150.1:n.4956-52T>C
XM_011538080.1:c.4956-52T>C	XP_011536382.1:n.4956-52T>C
XM_011538081.1:c.4953-52T>C	XP_011536383.1:n.4953-52T>C
XM_011538082.1:c.4926-52T>C	XP_011536384.1:n.4926-52T>C
XM_011538080.2:c.4956-52T>C	XP_011536382.1:n.4956-52T>C
XM_011538081.2:c.4953-52T>C	XP_011536383.1:n.4953-52T>C
XM_011538082.2:c.4926-52T>C	XP_011536384.1:n.4926-52T>C
XM_017019090.1:c.4953-52T>C	XP_016874579.1:n.4953-52T>C
NM_015335.5:c.4956-52T>C MANE Select	NP_056150.1:n.4956-52T>C