Canonical Allele Identifier: CA386888818

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429584T>G (hg19) ; chr12:g.115991779T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991779T>G , CM000674.2:g.115991779T>G	GRCh38
NC_000012.11:g.116429584T>G , CM000674.1:g.116429584T>G	GRCh37
NC_000012.10:g.114913967T>G	NCBI36
NG_023366.1:g.290408A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3175A>C MANE Select	ENSP00000281928.3:p.Thr1059Pro
ENST00000548743.2:c.3145A>C	ENSP00000448553.2:p.Thr1049Pro
ENST00000549786.2:c.2603A>C
ENST00000648173.1:n.1970A>C
ENST00000648379.1:n.1543A>C
ENST00000648737.1:n.2939A>C
ENST00000648916.1:n.1186A>C
ENST00000649607.1:c.1359A>C
ENST00000650226.1:c.3175A>C	ENSP00000496981.1:p.Thr1059Pro
ENST00000281928.7:c.3175A>C	ENSP00000281928.3:p.Thr1059Pro
NM_015335.4:c.3175A>C	NP_056150.1:p.Thr1059Pro
XM_011538080.1:c.3175A>C	XP_011536382.1:p.Thr1059Pro
XM_011538081.1:c.3172A>C	XP_011536383.1:p.Thr1058Pro
XM_011538082.1:c.3145A>C	XP_011536384.1:p.Thr1049Pro
XM_011538080.2:c.3175A>C	XP_011536382.1:p.Thr1059Pro
XM_011538081.2:c.3172A>C	XP_011536383.1:p.Thr1058Pro
XM_011538082.2:c.3145A>C	XP_011536384.1:p.Thr1049Pro
XM_017019090.1:c.3172A>C	XP_016874579.1:p.Thr1058Pro
NM_015335.5:c.3175A>C MANE Select	NP_056150.1:p.Thr1059Pro