Canonical Allele Identifier: CA386882218

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420382A>C (hg19) ; chr12:g.115982577A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982577A>C , CM000674.2:g.115982577A>C	GRCh38
NC_000012.11:g.116420382A>C , CM000674.1:g.116420382A>C	GRCh37
NC_000012.10:g.114904765A>C	NCBI36
NG_023366.1:g.299610T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4982T>G MANE Select	ENSP00000281928.3:p.Ile1661Ser
ENST00000549786.2:c.4410T>G
ENST00000648379.1:n.3350T>G
ENST00000648737.1:n.4746T>G
ENST00000648825.1:n.1722T>G
ENST00000648916.1:n.2993T>G
ENST00000649146.1:n.2225T>G
ENST00000649607.1:c.3166T>G
ENST00000649775.1:c.1471T>G
ENST00000650226.1:c.4982T>G	ENSP00000496981.1:p.Ile1661Ser
ENST00000281928.7:c.4982T>G	ENSP00000281928.3:p.Ile1661Ser
ENST00000549786.1:c.346T>G
ENST00000552340.1:c.14T>G	ENSP00000449876.1:p.Ile5Ser
NM_015335.4:c.4982T>G	NP_056150.1:p.Ile1661Ser
XM_011538080.1:c.4982T>G	XP_011536382.1:p.Ile1661Ser
XM_011538081.1:c.4979T>G	XP_011536383.1:p.Ile1660Ser
XM_011538082.1:c.4952T>G	XP_011536384.1:p.Ile1651Ser
XM_011538080.2:c.4982T>G	XP_011536382.1:p.Ile1661Ser
XM_011538081.2:c.4979T>G	XP_011536383.1:p.Ile1660Ser
XM_011538082.2:c.4952T>G	XP_011536384.1:p.Ile1651Ser
XM_017019090.1:c.4979T>G	XP_016874579.1:p.Ile1660Ser
NM_015335.5:c.4982T>G MANE Select	NP_056150.1:p.Ile1661Ser