Canonical Allele Identifier: CA482137253

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429483G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991678G>T , CM000674.2:g.115991678G>T	GRCh38
NC_000012.11:g.116429483G>T , CM000674.1:g.116429483G>T	GRCh37
NC_000012.10:g.114913866G>T	NCBI36
NG_023366.1:g.290509C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3276C>A MANE Select	ENSP00000281928.3:p.Leu1092=
ENST00000549786.2:c.2704C>A
ENST00000648379.1:n.1644C>A
ENST00000648737.1:n.3040C>A
ENST00000648825.1:n.16C>A
ENST00000648916.1:n.1287C>A
ENST00000649607.1:c.1460C>A
ENST00000650226.1:c.3276C>A	ENSP00000496981.1:p.Leu1092=
ENST00000281928.7:c.3276C>A	ENSP00000281928.3:p.Leu1092=
NM_015335.4:c.3276C>A	NP_056150.1:p.Leu1092=
XM_011538080.1:c.3276C>A	XP_011536382.1:p.Leu1092=
XM_011538081.1:c.3273C>A	XP_011536383.1:p.Leu1091=
XM_011538082.1:c.3246C>A	XP_011536384.1:p.Leu1082=
XM_011538080.2:c.3276C>A	XP_011536382.1:p.Leu1092=
XM_011538081.2:c.3273C>A	XP_011536383.1:p.Leu1091=
XM_011538082.2:c.3246C>A	XP_011536384.1:p.Leu1082=
XM_017019090.1:c.3273C>A	XP_016874579.1:p.Leu1091=
NM_015335.5:c.3276C>A MANE Select	NP_056150.1:p.Leu1092=