Canonical Allele Identifier: CA481946627

Gene: MED13L

Linked Data

• dbSNP Id: rs1250024557
• gnomAD v2: 12-116420348-G-A
• gnomAD v4: 12-115982543-G-A
• MyVariant Identifiers: chr12:g.116420348G>A (hg19) ; chr12:g.115982543G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982543G>A , CM000674.2:g.115982543G>A	GRCh38
NC_000012.11:g.116420348G>A , CM000674.1:g.116420348G>A	GRCh37
NC_000012.10:g.114904731G>A	NCBI36
NG_023366.1:g.299644C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5016C>T MANE Select	ENSP00000281928.3:p.Ala1672=
ENST00000549786.2:c.4444C>T
ENST00000648379.1:n.3384C>T
ENST00000648737.1:n.4780C>T
ENST00000648825.1:n.1756C>T
ENST00000648916.1:n.3027C>T
ENST00000649146.1:n.2259C>T
ENST00000649607.1:c.3200C>T
ENST00000649775.1:c.1505C>T
ENST00000650226.1:c.5016C>T	ENSP00000496981.1:p.Ala1672=
ENST00000281928.7:c.5016C>T	ENSP00000281928.3:p.Ala1672=
ENST00000549786.1:c.380C>T
ENST00000552340.1:c.48C>T	ENSP00000449876.1:p.Ala16=
NM_015335.4:c.5016C>T	NP_056150.1:p.Ala1672=
XM_011538080.1:c.5016C>T	XP_011536382.1:p.Ala1672=
XM_011538081.1:c.5013C>T	XP_011536383.1:p.Ala1671=
XM_011538082.1:c.4986C>T	XP_011536384.1:p.Ala1662=
XM_011538080.2:c.5016C>T	XP_011536382.1:p.Ala1672=
XM_011538081.2:c.5013C>T	XP_011536383.1:p.Ala1671=
XM_011538082.2:c.4986C>T	XP_011536384.1:p.Ala1662=
XM_017019090.1:c.5013C>T	XP_016874579.1:p.Ala1671=
NM_015335.5:c.5016C>T MANE Select	NP_056150.1:p.Ala1672=