Canonical Allele Identifier: CA386887804

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429347T>G (hg19) ; chr12:g.115991542T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991542T>G , CM000674.2:g.115991542T>G	GRCh38
NC_000012.11:g.116429347T>G , CM000674.1:g.116429347T>G	GRCh37
NC_000012.10:g.114913730T>G	NCBI36
NG_023366.1:g.290645A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3412A>C MANE Select	ENSP00000281928.3:p.Met1138Leu
ENST00000549786.2:c.2840A>C
ENST00000648379.1:n.1780A>C
ENST00000648737.1:n.3176A>C
ENST00000648825.1:n.152A>C
ENST00000648916.1:n.1423A>C
ENST00000649607.1:c.1596A>C
ENST00000650226.1:c.3412A>C	ENSP00000496981.1:p.Met1138Leu
ENST00000281928.7:c.3412A>C	ENSP00000281928.3:p.Met1138Leu
NM_015335.4:c.3412A>C	NP_056150.1:p.Met1138Leu
XM_011538080.1:c.3412A>C	XP_011536382.1:p.Met1138Leu
XM_011538081.1:c.3409A>C	XP_011536383.1:p.Met1137Leu
XM_011538082.1:c.3382A>C	XP_011536384.1:p.Met1128Leu
XM_011538080.2:c.3412A>C	XP_011536382.1:p.Met1138Leu
XM_011538081.2:c.3409A>C	XP_011536383.1:p.Met1137Leu
XM_011538082.2:c.3382A>C	XP_011536384.1:p.Met1128Leu
XM_017019090.1:c.3409A>C	XP_016874579.1:p.Met1137Leu
NM_015335.5:c.3412A>C MANE Select	NP_056150.1:p.Met1138Leu