Canonical Allele Identifier: CA386882238

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420385C>A (hg19) ; chr12:g.115982580C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982580C>A , CM000674.2:g.115982580C>A	GRCh38
NC_000012.11:g.116420385C>A , CM000674.1:g.116420385C>A	GRCh37
NC_000012.10:g.114904768C>A	NCBI36
NG_023366.1:g.299607G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4979G>T MANE Select	ENSP00000281928.3:p.Gly1660Val
ENST00000549786.2:c.4407G>T
ENST00000648379.1:n.3347G>T
ENST00000648737.1:n.4743G>T
ENST00000648825.1:n.1719G>T
ENST00000648916.1:n.2990G>T
ENST00000649146.1:n.2222G>T
ENST00000649607.1:c.3163G>T
ENST00000649775.1:c.1468G>T
ENST00000650226.1:c.4979G>T	ENSP00000496981.1:p.Gly1660Val
ENST00000281928.7:c.4979G>T	ENSP00000281928.3:p.Gly1660Val
ENST00000549786.1:c.343G>T
ENST00000552340.1:c.11G>T	ENSP00000449876.1:p.Gly4Val
NM_015335.4:c.4979G>T	NP_056150.1:p.Gly1660Val
XM_011538080.1:c.4979G>T	XP_011536382.1:p.Gly1660Val
XM_011538081.1:c.4976G>T	XP_011536383.1:p.Gly1659Val
XM_011538082.1:c.4949G>T	XP_011536384.1:p.Gly1650Val
XM_011538080.2:c.4979G>T	XP_011536382.1:p.Gly1660Val
XM_011538081.2:c.4976G>T	XP_011536383.1:p.Gly1659Val
XM_011538082.2:c.4949G>T	XP_011536384.1:p.Gly1650Val
XM_017019090.1:c.4976G>T	XP_016874579.1:p.Gly1659Val
NM_015335.5:c.4979G>T MANE Select	NP_056150.1:p.Gly1660Val