Canonical Allele Identifier: CA684026825

Gene: MED13L

Linked Data

• dbSNP Id: rs1197955755
• MyVariant Identifiers: chr12:g.116434588del (hg19) ; chr12:g.115996783del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115996785del , CM000674.2:g.115996785del	GRCh38
NC_000012.11:g.116434590del , CM000674.1:g.116434590del	GRCh37
NC_000012.10:g.114918973del	NCBI36
NG_023366.1:g.285404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2791-102del MANE Select	ENSP00000281928.3:n.2791-102del
ENST00000548743.2:c.2761-102del	ENSP00000448553.2:n.2761-102del
ENST00000549786.2:c.2219-102del
ENST00000647927.1:n.3164-102del
ENST00000648173.1:n.1586-102del
ENST00000648379.1:n.1159-102del
ENST00000648737.1:n.2555-102del
ENST00000648916.1:n.802-102del
ENST00000649607.1:c.975-102del
ENST00000650226.1:c.2791-102del	ENSP00000496981.1:n.2791-102del
ENST00000281928.7:c.2791-102del	ENSP00000281928.3:n.2791-102del
NM_015335.4:c.2791-102del	NP_056150.1:n.2791-102del
XM_011538080.1:c.2791-102del	XP_011536382.1:n.2791-102del
XM_011538081.1:c.2788-102del	XP_011536383.1:n.2788-102del
XM_011538082.1:c.2761-102del	XP_011536384.1:n.2761-102del
XM_011538080.2:c.2791-102del	XP_011536382.1:n.2791-102del
XM_011538081.2:c.2788-102del	XP_011536383.1:n.2788-102del
XM_011538082.2:c.2761-102del	XP_011536384.1:n.2761-102del
XM_017019090.1:c.2788-102del	XP_016874579.1:n.2788-102del
NM_015335.5:c.2791-102del MANE Select	NP_056150.1:n.2791-102del