Canonical Allele Identifier: CA6810994
Gene: MED13L HGNC NCBI

Linked Data

dbSNP Id: rs745891184

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115991642G>A , CM000674.2:g.115991642G>A GRCh38
NC_000012.11:g.116429447G>A , CM000674.1:g.116429447G>A GRCh37
NC_000012.10:g.114913830G>A NCBI36
NG_023366.1:g.290545C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281928.9:c.3312C>T MANE Select ENSP00000281928.3:p.Pro1104=
ENST00000549786.2:c.2740C>T
ENST00000648379.1:n.1680C>T
ENST00000648737.1:n.3076C>T
ENST00000648825.1:n.52C>T
ENST00000648916.1:n.1323C>T
ENST00000649607.1:c.1496C>T
ENST00000650226.1:c.3312C>T ENSP00000496981.1:p.Pro1104=
ENST00000281928.7:c.3312C>T ENSP00000281928.3:p.Pro1104=
NM_015335.4:c.3312C>T NP_056150.1:p.Pro1104=
XM_011538080.1:c.3312C>T XP_011536382.1:p.Pro1104=
XM_011538081.1:c.3309C>T XP_011536383.1:p.Pro1103=
XM_011538082.1:c.3282C>T XP_011536384.1:p.Pro1094=
XM_011538080.2:c.3312C>T XP_011536382.1:p.Pro1104=
XM_011538081.2:c.3309C>T XP_011536383.1:p.Pro1103=
XM_011538082.2:c.3282C>T XP_011536384.1:p.Pro1094=
XM_017019090.1:c.3309C>T XP_016874579.1:p.Pro1103=
NM_015335.5:c.3312C>T MANE Select NP_056150.1:p.Pro1104=