Canonical Allele Identifier: CA386890915

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116435029G>A (hg19) ; chr12:g.115997224G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997224G>A , CM000674.2:g.115997224G>A	GRCh38
NC_000012.11:g.116435029G>A , CM000674.1:g.116435029G>A	GRCh37
NC_000012.10:g.114919412G>A	NCBI36
NG_023366.1:g.284963C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.2576C>T MANE Select	ENSP00000281928.3:p.Ala859Val
ENST00000548743.2:c.2546C>T	ENSP00000448553.2:p.Ala849Val
ENST00000549786.2:c.2004C>T
ENST00000647927.1:n.2949C>T
ENST00000648173.1:n.1371C>T
ENST00000648379.1:n.944C>T
ENST00000648737.1:n.2340C>T
ENST00000648916.1:n.587C>T
ENST00000649607.1:c.760C>T
ENST00000650226.1:c.2576C>T	ENSP00000496981.1:p.Ala859Val
ENST00000281928.7:c.2576C>T	ENSP00000281928.3:p.Ala859Val
NM_015335.4:c.2576C>T	NP_056150.1:p.Ala859Val
XM_011538080.1:c.2576C>T	XP_011536382.1:p.Ala859Val
XM_011538081.1:c.2573C>T	XP_011536383.1:p.Ala858Val
XM_011538082.1:c.2546C>T	XP_011536384.1:p.Ala849Val
XM_011538080.2:c.2576C>T	XP_011536382.1:p.Ala859Val
XM_011538081.2:c.2573C>T	XP_011536383.1:p.Ala858Val
XM_011538082.2:c.2546C>T	XP_011536384.1:p.Ala849Val
XM_017019090.1:c.2573C>T	XP_016874579.1:p.Ala858Val
NM_015335.5:c.2576C>T MANE Select	NP_056150.1:p.Ala859Val