Canonical Allele Identifier: CA482137401

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429324G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991519G>T , CM000674.2:g.115991519G>T	GRCh38
NC_000012.11:g.116429324G>T , CM000674.1:g.116429324G>T	GRCh37
NC_000012.10:g.114913707G>T	NCBI36
NG_023366.1:g.290668C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3435C>A MANE Select	ENSP00000281928.3:p.Val1145=
ENST00000549786.2:c.2863C>A
ENST00000648379.1:n.1803C>A
ENST00000648737.1:n.3199C>A
ENST00000648825.1:n.175C>A
ENST00000648916.1:n.1446C>A
ENST00000649607.1:c.1619C>A
ENST00000650226.1:c.3435C>A	ENSP00000496981.1:p.Val1145=
ENST00000281928.7:c.3435C>A	ENSP00000281928.3:p.Val1145=
NM_015335.4:c.3435C>A	NP_056150.1:p.Val1145=
XM_011538080.1:c.3435C>A	XP_011536382.1:p.Val1145=
XM_011538081.1:c.3432C>A	XP_011536383.1:p.Val1144=
XM_011538082.1:c.3405C>A	XP_011536384.1:p.Val1135=
XM_011538080.2:c.3435C>A	XP_011536382.1:p.Val1145=
XM_011538081.2:c.3432C>A	XP_011536383.1:p.Val1144=
XM_011538082.2:c.3405C>A	XP_011536384.1:p.Val1135=
XM_017019090.1:c.3432C>A	XP_016874579.1:p.Val1144=
NM_015335.5:c.3435C>A MANE Select	NP_056150.1:p.Val1145=