Canonical Allele Identifier: CA386890666

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116434918C>T (hg19) ; chr12:g.115997113C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997113C>T , CM000674.2:g.115997113C>T	GRCh38
NC_000012.11:g.116434918C>T , CM000674.1:g.116434918C>T	GRCh37
NC_000012.10:g.114919301C>T	NCBI36
NG_023366.1:g.285074G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.2687G>A MANE Select	ENSP00000281928.3:p.Gly896Asp
ENST00000548743.2:c.2657G>A	ENSP00000448553.2:p.Gly886Asp
ENST00000549786.2:c.2115G>A
ENST00000647927.1:n.3060G>A
ENST00000648173.1:n.1482G>A
ENST00000648379.1:n.1055G>A
ENST00000648737.1:n.2451G>A
ENST00000648916.1:n.698G>A
ENST00000649607.1:c.871G>A
ENST00000650226.1:c.2687G>A	ENSP00000496981.1:p.Gly896Asp
ENST00000281928.7:c.2687G>A	ENSP00000281928.3:p.Gly896Asp
NM_015335.4:c.2687G>A	NP_056150.1:p.Gly896Asp
XM_011538080.1:c.2687G>A	XP_011536382.1:p.Gly896Asp
XM_011538081.1:c.2684G>A	XP_011536383.1:p.Gly895Asp
XM_011538082.1:c.2657G>A	XP_011536384.1:p.Gly886Asp
XM_011538080.2:c.2687G>A	XP_011536382.1:p.Gly896Asp
XM_011538081.2:c.2684G>A	XP_011536383.1:p.Gly895Asp
XM_011538082.2:c.2657G>A	XP_011536384.1:p.Gly886Asp
XM_017019090.1:c.2684G>A	XP_016874579.1:p.Gly895Asp
NM_015335.5:c.2687G>A MANE Select	NP_056150.1:p.Gly896Asp