Canonical Allele Identifier: CA2065396569
Gene: MED13L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115997024G= , CM000674.2:g.115997024G= GRCh38
NC_000012.11:g.116434829G= , CM000674.1:g.116434829G= GRCh37
NC_000012.10:g.114919212G= NCBI36
NG_023366.1:g.285163C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.2776C= MANE Select ENSP00000281928.3:p.Pro926=
ENST00000548743.2:c.2746C= ENSP00000448553.2:p.Pro916=
ENST00000549786.2:c.2204C=
ENST00000647927.1:n.3149C=
ENST00000648173.1:n.1571C=
ENST00000648379.1:n.1144C=
ENST00000648737.1:n.2540C=
ENST00000648916.1:n.787C=
ENST00000649607.1:c.960C=
ENST00000650226.1:c.2776C= ENSP00000496981.1:p.Pro926=
ENST00000281928.7:c.2776C= ENSP00000281928.3:p.Pro926=
NM_015335.4:c.2776C= NP_056150.1:p.Pro926=
XM_011538080.1:c.2776C= XP_011536382.1:p.Pro926=
XM_011538081.1:c.2773C= XP_011536383.1:p.Pro925=
XM_011538082.1:c.2746C= XP_011536384.1:p.Pro916=
XM_011538080.2:c.2776C= XP_011536382.1:p.Pro926=
XM_011538081.2:c.2773C= XP_011536383.1:p.Pro925=
XM_011538082.2:c.2746C= XP_011536384.1:p.Pro916=
XM_017019090.1:c.2773C= XP_016874579.1:p.Pro925=
NM_015335.5:c.2776C= MANE Select NP_056150.1:p.Pro926=