Canonical Allele Identifier: CA2065408837

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115966136C= , CM000674.2:g.115966136C=	GRCh38
NC_000012.11:g.116403941C= , CM000674.1:g.116403941C=	GRCh37
NC_000012.10:g.114888324C=	NCBI36
NG_023366.1:g.316051G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.6333G= MANE Select	ENSP00000281928.3:p.Gln2111=
ENST00000548784.2:n.2547G=
ENST00000648379.1:n.4701G=
ENST00000648737.1:n.6097G=
ENST00000648762.1:n.1023G=
ENST00000648825.1:n.4518G=
ENST00000648916.1:n.4344G=
ENST00000649607.1:c.4517G=
ENST00000649775.1:c.2664G=
ENST00000650226.1:c.6369G=	ENSP00000496981.1:p.Gln2123=
ENST00000281928.7:c.6333G=	ENSP00000281928.3:p.Gln2111=
NM_015335.4:c.6333G=	NP_056150.1:p.Gln2111=
XM_011538080.1:c.6369G=	XP_011536382.1:p.Gln2123=
XM_011538081.1:c.6366G=	XP_011536383.1:p.Gln2122=
XM_011538082.1:c.6339G=	XP_011536384.1:p.Gln2113=
XM_011538080.2:c.6369G=	XP_011536382.1:p.Gln2123=
XM_011538081.2:c.6366G=	XP_011536383.1:p.Gln2122=
XM_011538082.2:c.6339G=	XP_011536384.1:p.Gln2113=
XM_017019090.1:c.6330G=	XP_016874579.1:p.Gln2110=
NM_015335.5:c.6333G= MANE Select	NP_056150.1:p.Gln2111=