Canonical Allele Identifier: CA386887722

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429313A>C (hg19) ; chr12:g.115991508A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991508A>C , CM000674.2:g.115991508A>C	GRCh38
NC_000012.11:g.116429313A>C , CM000674.1:g.116429313A>C	GRCh37
NC_000012.10:g.114913696A>C	NCBI36
NG_023366.1:g.290679T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3446T>G MANE Select	ENSP00000281928.3:p.Ile1149Ser
ENST00000549786.2:c.2874T>G
ENST00000648379.1:n.1814T>G
ENST00000648737.1:n.3210T>G
ENST00000648825.1:n.186T>G
ENST00000648916.1:n.1457T>G
ENST00000649607.1:c.1630T>G
ENST00000650226.1:c.3446T>G	ENSP00000496981.1:p.Ile1149Ser
ENST00000281928.7:c.3446T>G	ENSP00000281928.3:p.Ile1149Ser
NM_015335.4:c.3446T>G	NP_056150.1:p.Ile1149Ser
XM_011538080.1:c.3446T>G	XP_011536382.1:p.Ile1149Ser
XM_011538081.1:c.3443T>G	XP_011536383.1:p.Ile1148Ser
XM_011538082.1:c.3416T>G	XP_011536384.1:p.Ile1139Ser
XM_011538080.2:c.3446T>G	XP_011536382.1:p.Ile1149Ser
XM_011538081.2:c.3443T>G	XP_011536383.1:p.Ile1148Ser
XM_011538082.2:c.3416T>G	XP_011536384.1:p.Ile1139Ser
XM_017019090.1:c.3443T>G	XP_016874579.1:p.Ile1148Ser
NM_015335.5:c.3446T>G MANE Select	NP_056150.1:p.Ile1149Ser