Canonical Allele Identifier: CA6810391

Gene: MED13L

Linked Data

• dbSNP Id: rs756339110
• ExAC: 12:116403863 C / A
• gnomAD v2: 12-116403863-C-A
• gnomAD v4: 12-115966058-C-A
• MyVariant Identifiers: chr12:g.116403863C>A (hg19) ; chr12:g.115966058C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115966058C>A , CM000674.2:g.115966058C>A	GRCh38
NC_000012.11:g.116403863C>A , CM000674.1:g.116403863C>A	GRCh37
NC_000012.10:g.114888246C>A	NCBI36
NG_023366.1:g.316129G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.6387+24G>T MANE Select	ENSP00000281928.3:n.6387+24G>T
ENST00000548784.2:n.2601+24G>T
ENST00000648379.1:n.4755+24G>T
ENST00000648737.1:n.6151+24G>T
ENST00000648762.1:n.1077+24G>T
ENST00000648825.1:n.4572+24G>T
ENST00000648916.1:n.4398+24G>T
ENST00000649607.1:c.4571+24G>T
ENST00000649775.1:c.2718+24G>T
ENST00000650226.1:c.6423+24G>T	ENSP00000496981.1:n.6423+24G>T
ENST00000281928.7:c.6387+24G>T	ENSP00000281928.3:n.6387+24G>T
NM_015335.4:c.6387+24G>T	NP_056150.1:n.6387+24G>T
XM_011538080.1:c.6423+24G>T	XP_011536382.1:n.6423+24G>T
XM_011538081.1:c.6420+24G>T	XP_011536383.1:n.6420+24G>T
XM_011538082.1:c.6393+24G>T	XP_011536384.1:n.6393+24G>T
XM_011538080.2:c.6423+24G>T	XP_011536382.1:n.6423+24G>T
XM_011538081.2:c.6420+24G>T	XP_011536383.1:n.6420+24G>T
XM_011538082.2:c.6393+24G>T	XP_011536384.1:n.6393+24G>T
XM_017019090.1:c.6384+24G>T	XP_016874579.1:n.6384+24G>T
NM_015335.5:c.6387+24G>T MANE Select	NP_056150.1:n.6387+24G>T