Canonical Allele Identifier: CA386881063

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420226T>G (hg19) ; chr12:g.115982421T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982421T>G , CM000674.2:g.115982421T>G	GRCh38
NC_000012.11:g.116420226T>G , CM000674.1:g.116420226T>G	GRCh37
NC_000012.10:g.114904609T>G	NCBI36
NG_023366.1:g.299766A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5138A>C MANE Select	ENSP00000281928.3:p.Asn1713Thr
ENST00000549786.2:c.4566A>C
ENST00000648379.1:n.3506A>C
ENST00000648737.1:n.4902A>C
ENST00000648825.1:n.1878A>C
ENST00000648916.1:n.3149A>C
ENST00000649146.1:n.2381A>C
ENST00000649607.1:c.3322A>C
ENST00000649775.1:c.1627A>C
ENST00000650226.1:c.5138A>C	ENSP00000496981.1:p.Asn1713Thr
ENST00000281928.7:c.5138A>C	ENSP00000281928.3:p.Asn1713Thr
ENST00000549786.1:c.502A>C
ENST00000552340.1:c.170A>C	ENSP00000449876.1:p.Asn57Thr
NM_015335.4:c.5138A>C	NP_056150.1:p.Asn1713Thr
XM_011538080.1:c.5138A>C	XP_011536382.1:p.Asn1713Thr
XM_011538081.1:c.5135A>C	XP_011536383.1:p.Asn1712Thr
XM_011538082.1:c.5108A>C	XP_011536384.1:p.Asn1703Thr
XM_011538080.2:c.5138A>C	XP_011536382.1:p.Asn1713Thr
XM_011538081.2:c.5135A>C	XP_011536383.1:p.Asn1712Thr
XM_011538082.2:c.5108A>C	XP_011536384.1:p.Asn1703Thr
XM_017019090.1:c.5135A>C	XP_016874579.1:p.Asn1712Thr
NM_015335.5:c.5138A>C MANE Select	NP_056150.1:p.Asn1713Thr