Canonical Allele Identifier: CA2065375333

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984289C= , CM000674.2:g.115984289C=	GRCh38
NC_000012.11:g.116422094C= , CM000674.1:g.116422094C=	GRCh37
NC_000012.10:g.114906477C=	NCBI36
NG_023366.1:g.297898G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4422G= MANE Select	ENSP00000281928.3:p.Lys1474=
ENST00000549786.2:c.3850G=
ENST00000648379.1:n.2790G=
ENST00000648737.1:n.4186G=
ENST00000648825.1:n.1162G=
ENST00000648916.1:n.2433G=
ENST00000649146.1:n.1152G=
ENST00000649607.1:c.2606G=
ENST00000649775.1:c.919G=
ENST00000650091.1:n.2398G=
ENST00000650226.1:c.4422G=	ENSP00000496981.1:p.Lys1474=
ENST00000281928.7:c.4422G=	ENSP00000281928.3:p.Lys1474=
NM_015335.4:c.4422G=	NP_056150.1:p.Lys1474=
XM_011538080.1:c.4422G=	XP_011536382.1:p.Lys1474=
XM_011538081.1:c.4419G=	XP_011536383.1:p.Lys1473=
XM_011538082.1:c.4392G=	XP_011536384.1:p.Lys1464=
XM_011538080.2:c.4422G=	XP_011536382.1:p.Lys1474=
XM_011538081.2:c.4419G=	XP_011536383.1:p.Lys1473=
XM_011538082.2:c.4392G=	XP_011536384.1:p.Lys1464=
XM_017019090.1:c.4419G=	XP_016874579.1:p.Lys1473=
NM_015335.5:c.4422G= MANE Select	NP_056150.1:p.Lys1474=