Canonical Allele Identifier: CA2621144724

Gene: MED13L

Linked Data

• gnomAD v4: 12-116002929-CACT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116002931_116002933del , CM000674.2:g.116002931_116002933del	GRCh38
NC_000012.11:g.116440736_116440738del , CM000674.1:g.116440736_116440738del	GRCh37
NC_000012.10:g.114925119_114925121del	NCBI36
NG_023366.1:g.279255_279257del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2569+71_2569+73del MANE Select	ENSP00000281928.3:n.2569+71_2569+73del
ENST00000548743.2:c.2539+71_2539+73del	ENSP00000448553.2:n.2539+71_2539+73del
ENST00000549786.2:c.1997+71_1997+73del
ENST00000648173.1:n.1364+71_1364+73del
ENST00000648379.1:n.937+71_937+73del
ENST00000648737.1:n.2333+71_2333+73del
ENST00000648916.1:n.580+71_580+73del
ENST00000649607.1:c.756+71_756+73del
ENST00000650226.1:c.2569+71_2569+73del	ENSP00000496981.1:n.2569+71_2569+73del
ENST00000281928.7:c.2569+71_2569+73del	ENSP00000281928.3:n.2569+71_2569+73del
NM_015335.4:c.2569+71_2569+73del	NP_056150.1:n.2569+71_2569+73del
XM_011538080.1:c.2569+71_2569+73del	XP_011536382.1:n.2569+71_2569+73del
XM_011538081.1:c.2569+71_2569+73del	XP_011536383.1:n.2569+71_2569+73del
XM_011538082.1:c.2539+71_2539+73del	XP_011536384.1:n.2539+71_2539+73del
XM_011538080.2:c.2569+71_2569+73del	XP_011536382.1:n.2569+71_2569+73del
XM_011538081.2:c.2569+71_2569+73del	XP_011536383.1:n.2569+71_2569+73del
XM_011538082.2:c.2539+71_2539+73del	XP_011536384.1:n.2539+71_2539+73del
XM_017019090.1:c.2569+71_2569+73del	XP_016874579.1:n.2569+71_2569+73del
NM_015335.5:c.2569+71_2569+73del MANE Select	NP_056150.1:n.2569+71_2569+73del