Canonical Allele Identifier: CA482137152

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429402C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991597C>G , CM000674.2:g.115991597C>G	GRCh38
NC_000012.11:g.116429402C>G , CM000674.1:g.116429402C>G	GRCh37
NC_000012.10:g.114913785C>G	NCBI36
NG_023366.1:g.290590G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3357G>C MANE Select	ENSP00000281928.3:p.Val1119=
ENST00000549786.2:c.2785G>C
ENST00000648379.1:n.1725G>C
ENST00000648737.1:n.3121G>C
ENST00000648825.1:n.97G>C
ENST00000648916.1:n.1368G>C
ENST00000649607.1:c.1541G>C
ENST00000650226.1:c.3357G>C	ENSP00000496981.1:p.Val1119=
ENST00000281928.7:c.3357G>C	ENSP00000281928.3:p.Val1119=
NM_015335.4:c.3357G>C	NP_056150.1:p.Val1119=
XM_011538080.1:c.3357G>C	XP_011536382.1:p.Val1119=
XM_011538081.1:c.3354G>C	XP_011536383.1:p.Val1118=
XM_011538082.1:c.3327G>C	XP_011536384.1:p.Val1109=
XM_011538080.2:c.3357G>C	XP_011536382.1:p.Val1119=
XM_011538081.2:c.3354G>C	XP_011536383.1:p.Val1118=
XM_011538082.2:c.3327G>C	XP_011536384.1:p.Val1109=
XM_017019090.1:c.3354G>C	XP_016874579.1:p.Val1118=
NM_015335.5:c.3357G>C MANE Select	NP_056150.1:p.Val1119=