Canonical Allele Identifier: CA386887965

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429392A>C (hg19) ; chr12:g.115991587A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991587A>C , CM000674.2:g.115991587A>C	GRCh38
NC_000012.11:g.116429392A>C , CM000674.1:g.116429392A>C	GRCh37
NC_000012.10:g.114913775A>C	NCBI36
NG_023366.1:g.290600T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.3367T>G MANE Select	ENSP00000281928.3:p.Phe1123Val
ENST00000549786.2:c.2795T>G
ENST00000648379.1:n.1735T>G
ENST00000648737.1:n.3131T>G
ENST00000648825.1:n.107T>G
ENST00000648916.1:n.1378T>G
ENST00000649607.1:c.1551T>G
ENST00000650226.1:c.3367T>G	ENSP00000496981.1:p.Phe1123Val
ENST00000281928.7:c.3367T>G	ENSP00000281928.3:p.Phe1123Val
NM_015335.4:c.3367T>G	NP_056150.1:p.Phe1123Val
XM_011538080.1:c.3367T>G	XP_011536382.1:p.Phe1123Val
XM_011538081.1:c.3364T>G	XP_011536383.1:p.Phe1122Val
XM_011538082.1:c.3337T>G	XP_011536384.1:p.Phe1113Val
XM_011538080.2:c.3367T>G	XP_011536382.1:p.Phe1123Val
XM_011538081.2:c.3364T>G	XP_011536383.1:p.Phe1122Val
XM_011538082.2:c.3337T>G	XP_011536384.1:p.Phe1113Val
XM_017019090.1:c.3364T>G	XP_016874579.1:p.Phe1122Val
NM_015335.5:c.3367T>G MANE Select	NP_056150.1:p.Phe1123Val