Canonical Allele Identifier: CA2065371641

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982524T= , CM000674.2:g.115982524T=	GRCh38
NC_000012.11:g.116420329T= , CM000674.1:g.116420329T=	GRCh37
NC_000012.10:g.114904712T=	NCBI36
NG_023366.1:g.299663A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5035A= MANE Select	ENSP00000281928.3:p.Ile1679=
ENST00000549786.2:c.4463A=
ENST00000648379.1:n.3403A=
ENST00000648737.1:n.4799A=
ENST00000648825.1:n.1775A=
ENST00000648916.1:n.3046A=
ENST00000649146.1:n.2278A=
ENST00000649607.1:c.3219A=
ENST00000649775.1:c.1524A=
ENST00000650226.1:c.5035A=	ENSP00000496981.1:p.Ile1679=
ENST00000281928.7:c.5035A=	ENSP00000281928.3:p.Ile1679=
ENST00000549786.1:c.399A=
ENST00000552340.1:c.67A=	ENSP00000449876.1:p.Ile23=
NM_015335.4:c.5035A=	NP_056150.1:p.Ile1679=
XM_011538080.1:c.5035A=	XP_011536382.1:p.Ile1679=
XM_011538081.1:c.5032A=	XP_011536383.1:p.Ile1678=
XM_011538082.1:c.5005A=	XP_011536384.1:p.Ile1669=
XM_011538080.2:c.5035A=	XP_011536382.1:p.Ile1679=
XM_011538081.2:c.5032A=	XP_011536383.1:p.Ile1678=
XM_011538082.2:c.5005A=	XP_011536384.1:p.Ile1669=
XM_017019090.1:c.5032A=	XP_016874579.1:p.Ile1678=
NM_015335.5:c.5035A= MANE Select	NP_056150.1:p.Ile1679=