Canonical Allele Identifier: CA2065408842

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115966146T= , CM000674.2:g.115966146T=	GRCh38
NC_000012.11:g.116403951T= , CM000674.1:g.116403951T=	GRCh37
NC_000012.10:g.114888334T=	NCBI36
NG_023366.1:g.316041A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.6323A= MANE Select	ENSP00000281928.3:p.Asn2108=
ENST00000548784.2:n.2537A=
ENST00000648379.1:n.4691A=
ENST00000648737.1:n.6087A=
ENST00000648762.1:n.1013A=
ENST00000648825.1:n.4508A=
ENST00000648916.1:n.4334A=
ENST00000649607.1:c.4507A=
ENST00000649775.1:c.2654A=
ENST00000650226.1:c.6359A=	ENSP00000496981.1:p.Asn2120=
ENST00000281928.7:c.6323A=	ENSP00000281928.3:p.Asn2108=
NM_015335.4:c.6323A=	NP_056150.1:p.Asn2108=
XM_011538080.1:c.6359A=	XP_011536382.1:p.Asn2120=
XM_011538081.1:c.6356A=	XP_011536383.1:p.Asn2119=
XM_011538082.1:c.6329A=	XP_011536384.1:p.Asn2110=
XM_011538080.2:c.6359A=	XP_011536382.1:p.Asn2120=
XM_011538081.2:c.6356A=	XP_011536383.1:p.Asn2119=
XM_011538082.2:c.6329A=	XP_011536384.1:p.Asn2110=
XM_017019090.1:c.6320A=	XP_016874579.1:p.Asn2107=
NM_015335.5:c.6323A= MANE Select	NP_056150.1:p.Asn2108=