Canonical Allele Identifier: CA386887835

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429360G>C (hg19) ; chr12:g.115991555G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991555G>C , CM000674.2:g.115991555G>C	GRCh38
NC_000012.11:g.116429360G>C , CM000674.1:g.116429360G>C	GRCh37
NC_000012.10:g.114913743G>C	NCBI36
NG_023366.1:g.290632C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3399C>G MANE Select	ENSP00000281928.3:p.Ile1133Met
ENST00000549786.2:c.2827C>G
ENST00000648379.1:n.1767C>G
ENST00000648737.1:n.3163C>G
ENST00000648825.1:n.139C>G
ENST00000648916.1:n.1410C>G
ENST00000649607.1:c.1583C>G
ENST00000650226.1:c.3399C>G	ENSP00000496981.1:p.Ile1133Met
ENST00000281928.7:c.3399C>G	ENSP00000281928.3:p.Ile1133Met
NM_015335.4:c.3399C>G	NP_056150.1:p.Ile1133Met
XM_011538080.1:c.3399C>G	XP_011536382.1:p.Ile1133Met
XM_011538081.1:c.3396C>G	XP_011536383.1:p.Ile1132Met
XM_011538082.1:c.3369C>G	XP_011536384.1:p.Ile1123Met
XM_011538080.2:c.3399C>G	XP_011536382.1:p.Ile1133Met
XM_011538081.2:c.3396C>G	XP_011536383.1:p.Ile1132Met
XM_011538082.2:c.3369C>G	XP_011536384.1:p.Ile1123Met
XM_017019090.1:c.3396C>G	XP_016874579.1:p.Ile1132Met
NM_015335.5:c.3399C>G MANE Select	NP_056150.1:p.Ile1133Met