Canonical Allele Identifier: CA481948969

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429747A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991942A>C , CM000674.2:g.115991942A>C	GRCh38
NC_000012.11:g.116429747A>C , CM000674.1:g.116429747A>C	GRCh37
NC_000012.10:g.114914130A>C	NCBI36
NG_023366.1:g.290245T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3012T>G MANE Select	ENSP00000281928.3:p.Val1004=
ENST00000548743.2:c.2982T>G	ENSP00000448553.2:p.Val994=
ENST00000549786.2:c.2440T>G
ENST00000648173.1:n.1807T>G
ENST00000648379.1:n.1380T>G
ENST00000648737.1:n.2776T>G
ENST00000648916.1:n.1023T>G
ENST00000649607.1:c.1196T>G
ENST00000650226.1:c.3012T>G	ENSP00000496981.1:p.Val1004=
ENST00000281928.7:c.3012T>G	ENSP00000281928.3:p.Val1004=
NM_015335.4:c.3012T>G	NP_056150.1:p.Val1004=
XM_011538080.1:c.3012T>G	XP_011536382.1:p.Val1004=
XM_011538081.1:c.3009T>G	XP_011536383.1:p.Val1003=
XM_011538082.1:c.2982T>G	XP_011536384.1:p.Val994=
XM_011538080.2:c.3012T>G	XP_011536382.1:p.Val1004=
XM_011538081.2:c.3009T>G	XP_011536383.1:p.Val1003=
XM_011538082.2:c.2982T>G	XP_011536384.1:p.Val994=
XM_017019090.1:c.3009T>G	XP_016874579.1:p.Val1003=
NM_015335.5:c.3012T>G MANE Select	NP_056150.1:p.Val1004=