Canonical Allele Identifier: CA386876102

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116408414A>C (hg19) ; chr12:g.115970609A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115970609A>C , CM000674.2:g.115970609A>C	GRCh38
NC_000012.11:g.116408414A>C , CM000674.1:g.116408414A>C	GRCh37
NC_000012.10:g.114892797A>C	NCBI36
NG_023366.1:g.311578T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.6052T>G MANE Select	ENSP00000281928.3:p.Phe2018Val
ENST00000548784.2:n.2266T>G
ENST00000648379.1:n.4420T>G
ENST00000648737.1:n.5816T>G
ENST00000648825.1:n.4237T>G
ENST00000648916.1:n.4063T>G
ENST00000649607.1:c.4236T>G
ENST00000649775.1:c.2541T>G
ENST00000650226.1:c.6088T>G	ENSP00000496981.1:p.Phe2030Val
ENST00000281928.7:c.6052T>G	ENSP00000281928.3:p.Phe2018Val
NM_015335.4:c.6052T>G	NP_056150.1:p.Phe2018Val
XM_011538080.1:c.6088T>G	XP_011536382.1:p.Phe2030Val
XM_011538081.1:c.6085T>G	XP_011536383.1:p.Phe2029Val
XM_011538082.1:c.6058T>G	XP_011536384.1:p.Phe2020Val
XM_011538080.2:c.6088T>G	XP_011536382.1:p.Phe2030Val
XM_011538081.2:c.6085T>G	XP_011536383.1:p.Phe2029Val
XM_011538082.2:c.6058T>G	XP_011536384.1:p.Phe2020Val
XM_017019090.1:c.6049T>G	XP_016874579.1:p.Phe2017Val
NM_015335.5:c.6052T>G MANE Select	NP_056150.1:p.Phe2018Val