Canonical Allele Identifier: CA2065396708

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997102T= , CM000674.2:g.115997102T=	GRCh38
NC_000012.11:g.116434907T= , CM000674.1:g.116434907T=	GRCh37
NC_000012.10:g.114919290T=	NCBI36
NG_023366.1:g.285085A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2698A= MANE Select	ENSP00000281928.3:p.Ser900=
ENST00000548743.2:c.2668A=	ENSP00000448553.2:p.Ser890=
ENST00000549786.2:c.2126A=
ENST00000647927.1:n.3071A=
ENST00000648173.1:n.1493A=
ENST00000648379.1:n.1066A=
ENST00000648737.1:n.2462A=
ENST00000648916.1:n.709A=
ENST00000649607.1:c.882A=
ENST00000650226.1:c.2698A=	ENSP00000496981.1:p.Ser900=
ENST00000281928.7:c.2698A=	ENSP00000281928.3:p.Ser900=
NM_015335.4:c.2698A=	NP_056150.1:p.Ser900=
XM_011538080.1:c.2698A=	XP_011536382.1:p.Ser900=
XM_011538081.1:c.2695A=	XP_011536383.1:p.Ser899=
XM_011538082.1:c.2668A=	XP_011536384.1:p.Ser890=
XM_011538080.2:c.2698A=	XP_011536382.1:p.Ser900=
XM_011538081.2:c.2695A=	XP_011536383.1:p.Ser899=
XM_011538082.2:c.2668A=	XP_011536384.1:p.Ser890=
XM_017019090.1:c.2695A=	XP_016874579.1:p.Ser899=
NM_015335.5:c.2698A= MANE Select	NP_056150.1:p.Ser900=