Canonical Allele Identifier: CA2580085842

Gene: MED13L

Linked Data

• ClinVar Variation Id: 2033610
• ClinVar RCV Id: RCV002872504

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116002987A>T , CM000674.2:g.116002987A>T	GRCh38
NC_000012.11:g.116440792A>T , CM000674.1:g.116440792A>T	GRCh37
NC_000012.10:g.114925175A>T	NCBI36
NG_023366.1:g.279200T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2569+16T>A MANE Select	ENSP00000281928.3:n.2569+16T>A
ENST00000548743.2:c.2539+16T>A	ENSP00000448553.2:n.2539+16T>A
ENST00000549786.2:c.1997+16T>A
ENST00000648173.1:n.1364+16T>A
ENST00000648379.1:n.937+16T>A
ENST00000648737.1:n.2333+16T>A
ENST00000648916.1:n.580+16T>A
ENST00000649607.1:c.756+16T>A
ENST00000650226.1:c.2569+16T>A	ENSP00000496981.1:n.2569+16T>A
ENST00000281928.7:c.2569+16T>A	ENSP00000281928.3:n.2569+16T>A
NM_015335.4:c.2569+16T>A	NP_056150.1:n.2569+16T>A
XM_011538080.1:c.2569+16T>A	XP_011536382.1:n.2569+16T>A
XM_011538081.1:c.2569+16T>A	XP_011536383.1:n.2569+16T>A
XM_011538082.1:c.2539+16T>A	XP_011536384.1:n.2539+16T>A
XM_011538080.2:c.2569+16T>A	XP_011536382.1:n.2569+16T>A
XM_011538081.2:c.2569+16T>A	XP_011536383.1:n.2569+16T>A
XM_011538082.2:c.2539+16T>A	XP_011536384.1:n.2539+16T>A
XM_017019090.1:c.2569+16T>A	XP_016874579.1:n.2569+16T>A
NM_015335.5:c.2569+16T>A MANE Select	NP_056150.1:n.2569+16T>A