Canonical Allele Identifier: CA2621144504

Gene: MED13L

Linked Data

• gnomAD v4: 12-115996823-G-GAT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115996823_115996824insAT , CM000674.2:g.115996823_115996824insAT	GRCh38
NC_000012.11:g.116434628_116434629insAT , CM000674.1:g.116434628_116434629insAT	GRCh37
NC_000012.10:g.114919011_114919012insAT	NCBI36
NG_023366.1:g.285363_285364insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2791-143_2791-142insAT MANE Select	ENSP00000281928.3:n.2791-143_2791-142insAT
ENST00000548743.2:c.2761-143_2761-142insAT	ENSP00000448553.2:n.2761-143_2761-142insAT
ENST00000549786.2:c.2219-143_2219-142insAT
ENST00000647927.1:n.3164-143_3164-142insAT
ENST00000648173.1:n.1586-143_1586-142insAT
ENST00000648379.1:n.1159-143_1159-142insAT
ENST00000648737.1:n.2555-143_2555-142insAT
ENST00000648916.1:n.802-143_802-142insAT
ENST00000649607.1:c.975-143_975-142insAT
ENST00000650226.1:c.2791-143_2791-142insAT	ENSP00000496981.1:n.2791-143_2791-142insAT
ENST00000281928.7:c.2791-143_2791-142insAT	ENSP00000281928.3:n.2791-143_2791-142insAT
NM_015335.4:c.2791-143_2791-142insAT	NP_056150.1:n.2791-143_2791-142insAT
XM_011538080.1:c.2791-143_2791-142insAT	XP_011536382.1:n.2791-143_2791-142insAT
XM_011538081.1:c.2788-143_2788-142insAT	XP_011536383.1:n.2788-143_2788-142insAT
XM_011538082.1:c.2761-143_2761-142insAT	XP_011536384.1:n.2761-143_2761-142insAT
XM_011538080.2:c.2791-143_2791-142insAT	XP_011536382.1:n.2791-143_2791-142insAT
XM_011538081.2:c.2788-143_2788-142insAT	XP_011536383.1:n.2788-143_2788-142insAT
XM_011538082.2:c.2761-143_2761-142insAT	XP_011536384.1:n.2761-143_2761-142insAT
XM_017019090.1:c.2788-143_2788-142insAT	XP_016874579.1:n.2788-143_2788-142insAT
NM_015335.5:c.2791-143_2791-142insAT MANE Select	NP_056150.1:n.2791-143_2791-142insAT