Canonical Allele Identifier: CA386888635

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429533T>G (hg19) ; chr12:g.115991728T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991728T>G , CM000674.2:g.115991728T>G	GRCh38
NC_000012.11:g.116429533T>G , CM000674.1:g.116429533T>G	GRCh37
NC_000012.10:g.114913916T>G	NCBI36
NG_023366.1:g.290459A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3226A>C MANE Select	ENSP00000281928.3:p.Ser1076Arg
ENST00000548743.2:c.3196A>C	ENSP00000448553.2:p.Ser1066Arg
ENST00000549786.2:c.2654A>C
ENST00000648173.1:n.2021A>C
ENST00000648379.1:n.1594A>C
ENST00000648737.1:n.2990A>C
ENST00000648916.1:n.1237A>C
ENST00000649607.1:c.1410A>C
ENST00000650226.1:c.3226A>C	ENSP00000496981.1:p.Ser1076Arg
ENST00000281928.7:c.3226A>C	ENSP00000281928.3:p.Ser1076Arg
NM_015335.4:c.3226A>C	NP_056150.1:p.Ser1076Arg
XM_011538080.1:c.3226A>C	XP_011536382.1:p.Ser1076Arg
XM_011538081.1:c.3223A>C	XP_011536383.1:p.Ser1075Arg
XM_011538082.1:c.3196A>C	XP_011536384.1:p.Ser1066Arg
XM_011538080.2:c.3226A>C	XP_011536382.1:p.Ser1076Arg
XM_011538081.2:c.3223A>C	XP_011536383.1:p.Ser1075Arg
XM_011538082.2:c.3196A>C	XP_011536384.1:p.Ser1066Arg
XM_017019090.1:c.3223A>C	XP_016874579.1:p.Ser1075Arg
NM_015335.5:c.3226A>C MANE Select	NP_056150.1:p.Ser1076Arg