Canonical Allele Identifier: CA481949545

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116434896G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997091G>C , CM000674.2:g.115997091G>C	GRCh38
NC_000012.11:g.116434896G>C , CM000674.1:g.116434896G>C	GRCh37
NC_000012.10:g.114919279G>C	NCBI36
NG_023366.1:g.285096C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2709C>G MANE Select	ENSP00000281928.3:p.Val903=
ENST00000548743.2:c.2679C>G	ENSP00000448553.2:p.Val893=
ENST00000549786.2:c.2137C>G
ENST00000647927.1:n.3082C>G
ENST00000648173.1:n.1504C>G
ENST00000648379.1:n.1077C>G
ENST00000648737.1:n.2473C>G
ENST00000648916.1:n.720C>G
ENST00000649607.1:c.893C>G
ENST00000650226.1:c.2709C>G	ENSP00000496981.1:p.Val903=
ENST00000281928.7:c.2709C>G	ENSP00000281928.3:p.Val903=
NM_015335.4:c.2709C>G	NP_056150.1:p.Val903=
XM_011538080.1:c.2709C>G	XP_011536382.1:p.Val903=
XM_011538081.1:c.2706C>G	XP_011536383.1:p.Val902=
XM_011538082.1:c.2679C>G	XP_011536384.1:p.Val893=
XM_011538080.2:c.2709C>G	XP_011536382.1:p.Val903=
XM_011538081.2:c.2706C>G	XP_011536383.1:p.Val902=
XM_011538082.2:c.2679C>G	XP_011536384.1:p.Val893=
XM_017019090.1:c.2706C>G	XP_016874579.1:p.Val902=
NM_015335.5:c.2709C>G MANE Select	NP_056150.1:p.Val903=