Canonical Allele Identifier: CA481933612

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116460337A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116022532A>G , CM000674.2:g.116022532A>G	GRCh38
NC_000012.11:g.116460337A>G , CM000674.1:g.116460337A>G	GRCh37
NC_000012.10:g.114944720A>G	NCBI36
NG_023366.1:g.259655T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.549T>C MANE Select	ENSP00000281928.3:p.Ile183=
ENST00000548743.2:c.519T>C	ENSP00000448553.2:p.Ile173=
ENST00000647567.1:c.459T>C	ENSP00000497136.1:p.Ile153=
ENST00000648737.1:n.313T>C
ENST00000650226.1:c.549T>C	ENSP00000496981.1:p.Ile183=
ENST00000281928.7:c.549T>C	ENSP00000281928.3:p.Ile183=
NM_015335.4:c.549T>C	NP_056150.1:p.Ile183=
XM_011538080.1:c.549T>C	XP_011536382.1:p.Ile183=
XM_011538081.1:c.549T>C	XP_011536383.1:p.Ile183=
XM_011538082.1:c.519T>C	XP_011536384.1:p.Ile173=
XM_011538080.2:c.549T>C	XP_011536382.1:p.Ile183=
XM_011538081.2:c.549T>C	XP_011536383.1:p.Ile183=
XM_011538082.2:c.519T>C	XP_011536384.1:p.Ile173=
XM_017019090.1:c.549T>C	XP_016874579.1:p.Ile183=
NM_015335.5:c.549T>C MANE Select	NP_056150.1:p.Ile183=