Canonical Allele Identifier: CA386888016

Gene: MED13L

Linked Data

• gnomAD v4: 12-115991596-T-C
• MyVariant Identifiers: chr12:g.116429401T>C (hg19) ; chr12:g.115991596T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991596T>C , CM000674.2:g.115991596T>C	GRCh38
NC_000012.11:g.116429401T>C , CM000674.1:g.116429401T>C	GRCh37
NC_000012.10:g.114913784T>C	NCBI36
NG_023366.1:g.290591A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.3358A>G MANE Select	ENSP00000281928.3:p.Met1120Val
ENST00000549786.2:c.2786A>G
ENST00000648379.1:n.1726A>G
ENST00000648737.1:n.3122A>G
ENST00000648825.1:n.98A>G
ENST00000648916.1:n.1369A>G
ENST00000649607.1:c.1542A>G
ENST00000650226.1:c.3358A>G	ENSP00000496981.1:p.Met1120Val
ENST00000281928.7:c.3358A>G	ENSP00000281928.3:p.Met1120Val
NM_015335.4:c.3358A>G	NP_056150.1:p.Met1120Val
XM_011538080.1:c.3358A>G	XP_011536382.1:p.Met1120Val
XM_011538081.1:c.3355A>G	XP_011536383.1:p.Met1119Val
XM_011538082.1:c.3328A>G	XP_011536384.1:p.Met1110Val
XM_011538080.2:c.3358A>G	XP_011536382.1:p.Met1120Val
XM_011538081.2:c.3355A>G	XP_011536383.1:p.Met1119Val
XM_011538082.2:c.3328A>G	XP_011536384.1:p.Met1110Val
XM_017019090.1:c.3355A>G	XP_016874579.1:p.Met1119Val
NM_015335.5:c.3358A>G MANE Select	NP_056150.1:p.Met1120Val