Canonical Allele Identifier: CA482137129

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429378G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991573G>A , CM000674.2:g.115991573G>A	GRCh38
NC_000012.11:g.116429378G>A , CM000674.1:g.116429378G>A	GRCh37
NC_000012.10:g.114913761G>A	NCBI36
NG_023366.1:g.290614C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3381C>T MANE Select	ENSP00000281928.3:p.Asn1127=
ENST00000549786.2:c.2809C>T
ENST00000648379.1:n.1749C>T
ENST00000648737.1:n.3145C>T
ENST00000648825.1:n.121C>T
ENST00000648916.1:n.1392C>T
ENST00000649607.1:c.1565C>T
ENST00000650226.1:c.3381C>T	ENSP00000496981.1:p.Asn1127=
ENST00000281928.7:c.3381C>T	ENSP00000281928.3:p.Asn1127=
NM_015335.4:c.3381C>T	NP_056150.1:p.Asn1127=
XM_011538080.1:c.3381C>T	XP_011536382.1:p.Asn1127=
XM_011538081.1:c.3378C>T	XP_011536383.1:p.Asn1126=
XM_011538082.1:c.3351C>T	XP_011536384.1:p.Asn1117=
XM_011538080.2:c.3381C>T	XP_011536382.1:p.Asn1127=
XM_011538081.2:c.3378C>T	XP_011536383.1:p.Asn1126=
XM_011538082.2:c.3351C>T	XP_011536384.1:p.Asn1117=
XM_017019090.1:c.3378C>T	XP_016874579.1:p.Asn1126=
NM_015335.5:c.3381C>T MANE Select	NP_056150.1:p.Asn1127=