Canonical Allele Identifier: CA2065396697

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997096T= , CM000674.2:g.115997096T=	GRCh38
NC_000012.11:g.116434901T= , CM000674.1:g.116434901T=	GRCh37
NC_000012.10:g.114919284T=	NCBI36
NG_023366.1:g.285091A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2704A= MANE Select	ENSP00000281928.3:p.Met902=
ENST00000548743.2:c.2674A=	ENSP00000448553.2:p.Met892=
ENST00000549786.2:c.2132A=
ENST00000647927.1:n.3077A=
ENST00000648173.1:n.1499A=
ENST00000648379.1:n.1072A=
ENST00000648737.1:n.2468A=
ENST00000648916.1:n.715A=
ENST00000649607.1:c.888A=
ENST00000650226.1:c.2704A=	ENSP00000496981.1:p.Met902=
ENST00000281928.7:c.2704A=	ENSP00000281928.3:p.Met902=
NM_015335.4:c.2704A=	NP_056150.1:p.Met902=
XM_011538080.1:c.2704A=	XP_011536382.1:p.Met902=
XM_011538081.1:c.2701A=	XP_011536383.1:p.Met901=
XM_011538082.1:c.2674A=	XP_011536384.1:p.Met892=
XM_011538080.2:c.2704A=	XP_011536382.1:p.Met902=
XM_011538081.2:c.2701A=	XP_011536383.1:p.Met901=
XM_011538082.2:c.2674A=	XP_011536384.1:p.Met892=
XM_017019090.1:c.2701A=	XP_016874579.1:p.Met901=
NM_015335.5:c.2704A= MANE Select	NP_056150.1:p.Met902=