Canonical Allele Identifier: CA607654204

Gene: MED13L

Linked Data

• dbSNP Id: rs1456485648
• gnomAD v2: 12-116440669-T-C
• gnomAD v3: 12-116002864-T-C
• gnomAD v4: 12-116002864-T-C
• MyVariant Identifiers: chr12:g.116440669T>C (hg19) ; chr12:g.116002864T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116002864T>C , CM000674.2:g.116002864T>C	GRCh38
NC_000012.11:g.116440669T>C , CM000674.1:g.116440669T>C	GRCh37
NC_000012.10:g.114925052T>C	NCBI36
NG_023366.1:g.279323A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2569+139A>G MANE Select	ENSP00000281928.3:n.2569+139A>G
ENST00000548743.2:c.2539+139A>G	ENSP00000448553.2:n.2539+139A>G
ENST00000549786.2:c.1997+139A>G
ENST00000648173.1:n.1364+139A>G
ENST00000648379.1:n.937+139A>G
ENST00000648737.1:n.2333+139A>G
ENST00000648916.1:n.580+139A>G
ENST00000649607.1:c.756+139A>G
ENST00000650226.1:c.2569+139A>G	ENSP00000496981.1:n.2569+139A>G
ENST00000281928.7:c.2569+139A>G	ENSP00000281928.3:n.2569+139A>G
NM_015335.4:c.2569+139A>G	NP_056150.1:n.2569+139A>G
XM_011538080.1:c.2569+139A>G	XP_011536382.1:n.2569+139A>G
XM_011538081.1:c.2569+139A>G	XP_011536383.1:n.2569+139A>G
XM_011538082.1:c.2539+139A>G	XP_011536384.1:n.2539+139A>G
XM_011538080.2:c.2569+139A>G	XP_011536382.1:n.2569+139A>G
XM_011538081.2:c.2569+139A>G	XP_011536383.1:n.2569+139A>G
XM_011538082.2:c.2539+139A>G	XP_011536384.1:n.2539+139A>G
XM_017019090.1:c.2569+139A>G	XP_016874579.1:n.2569+139A>G
NM_015335.5:c.2569+139A>G MANE Select	NP_056150.1:n.2569+139A>G