Canonical Allele Identifier: CA386890691

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116434930A>G (hg19) ; chr12:g.115997125A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997125A>G , CM000674.2:g.115997125A>G	GRCh38
NC_000012.11:g.116434930A>G , CM000674.1:g.116434930A>G	GRCh37
NC_000012.10:g.114919313A>G	NCBI36
NG_023366.1:g.285062T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2675T>C MANE Select	ENSP00000281928.3:p.Val892Ala
ENST00000548743.2:c.2645T>C	ENSP00000448553.2:p.Val882Ala
ENST00000549786.2:c.2103T>C
ENST00000647927.1:n.3048T>C
ENST00000648173.1:n.1470T>C
ENST00000648379.1:n.1043T>C
ENST00000648737.1:n.2439T>C
ENST00000648916.1:n.686T>C
ENST00000649607.1:c.859T>C
ENST00000650226.1:c.2675T>C	ENSP00000496981.1:p.Val892Ala
ENST00000281928.7:c.2675T>C	ENSP00000281928.3:p.Val892Ala
NM_015335.4:c.2675T>C	NP_056150.1:p.Val892Ala
XM_011538080.1:c.2675T>C	XP_011536382.1:p.Val892Ala
XM_011538081.1:c.2672T>C	XP_011536383.1:p.Val891Ala
XM_011538082.1:c.2645T>C	XP_011536384.1:p.Val882Ala
XM_011538080.2:c.2675T>C	XP_011536382.1:p.Val892Ala
XM_011538081.2:c.2672T>C	XP_011536383.1:p.Val891Ala
XM_011538082.2:c.2645T>C	XP_011536384.1:p.Val882Ala
XM_017019090.1:c.2672T>C	XP_016874579.1:p.Val891Ala
NM_015335.5:c.2675T>C MANE Select	NP_056150.1:p.Val892Ala