Canonical Allele Identifier: CA481946583

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420339T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982534T>G , CM000674.2:g.115982534T>G	GRCh38
NC_000012.11:g.116420339T>G , CM000674.1:g.116420339T>G	GRCh37
NC_000012.10:g.114904722T>G	NCBI36
NG_023366.1:g.299653A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5025A>C MANE Select	ENSP00000281928.3:p.Pro1675=
ENST00000549786.2:c.4453A>C
ENST00000648379.1:n.3393A>C
ENST00000648737.1:n.4789A>C
ENST00000648825.1:n.1765A>C
ENST00000648916.1:n.3036A>C
ENST00000649146.1:n.2268A>C
ENST00000649607.1:c.3209A>C
ENST00000649775.1:c.1514A>C
ENST00000650226.1:c.5025A>C	ENSP00000496981.1:p.Pro1675=
ENST00000281928.7:c.5025A>C	ENSP00000281928.3:p.Pro1675=
ENST00000549786.1:c.389A>C
ENST00000552340.1:c.57A>C	ENSP00000449876.1:p.Pro19=
NM_015335.4:c.5025A>C	NP_056150.1:p.Pro1675=
XM_011538080.1:c.5025A>C	XP_011536382.1:p.Pro1675=
XM_011538081.1:c.5022A>C	XP_011536383.1:p.Pro1674=
XM_011538082.1:c.4995A>C	XP_011536384.1:p.Pro1665=
XM_011538080.2:c.5025A>C	XP_011536382.1:p.Pro1675=
XM_011538081.2:c.5022A>C	XP_011536383.1:p.Pro1674=
XM_011538082.2:c.4995A>C	XP_011536384.1:p.Pro1665=
XM_017019090.1:c.5022A>C	XP_016874579.1:p.Pro1674=
NM_015335.5:c.5025A>C MANE Select	NP_056150.1:p.Pro1675=