Canonical Allele Identifier: CA481949553

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116434917G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997112G>C , CM000674.2:g.115997112G>C	GRCh38
NC_000012.11:g.116434917G>C , CM000674.1:g.116434917G>C	GRCh37
NC_000012.10:g.114919300G>C	NCBI36
NG_023366.1:g.285075C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.2688C>G MANE Select	ENSP00000281928.3:p.Gly896=
ENST00000548743.2:c.2658C>G	ENSP00000448553.2:p.Gly886=
ENST00000549786.2:c.2116C>G
ENST00000647927.1:n.3061C>G
ENST00000648173.1:n.1483C>G
ENST00000648379.1:n.1056C>G
ENST00000648737.1:n.2452C>G
ENST00000648916.1:n.699C>G
ENST00000649607.1:c.872C>G
ENST00000650226.1:c.2688C>G	ENSP00000496981.1:p.Gly896=
ENST00000281928.7:c.2688C>G	ENSP00000281928.3:p.Gly896=
NM_015335.4:c.2688C>G	NP_056150.1:p.Gly896=
XM_011538080.1:c.2688C>G	XP_011536382.1:p.Gly896=
XM_011538081.1:c.2685C>G	XP_011536383.1:p.Gly895=
XM_011538082.1:c.2658C>G	XP_011536384.1:p.Gly886=
XM_011538080.2:c.2688C>G	XP_011536382.1:p.Gly896=
XM_011538081.2:c.2685C>G	XP_011536383.1:p.Gly895=
XM_011538082.2:c.2658C>G	XP_011536384.1:p.Gly886=
XM_017019090.1:c.2685C>G	XP_016874579.1:p.Gly895=
NM_015335.5:c.2688C>G MANE Select	NP_056150.1:p.Gly896=