Canonical Allele Identifier: CA386881265

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116420314G>A (hg19) ; chr12:g.115982509G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982509G>A , CM000674.2:g.115982509G>A	GRCh38
NC_000012.11:g.116420314G>A , CM000674.1:g.116420314G>A	GRCh37
NC_000012.10:g.114904697G>A	NCBI36
NG_023366.1:g.299678C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.5050C>T MANE Select	ENSP00000281928.3:p.Pro1684Ser
ENST00000549786.2:c.4478C>T
ENST00000648379.1:n.3418C>T
ENST00000648737.1:n.4814C>T
ENST00000648825.1:n.1790C>T
ENST00000648916.1:n.3061C>T
ENST00000649146.1:n.2293C>T
ENST00000649607.1:c.3234C>T
ENST00000649775.1:c.1539C>T
ENST00000650226.1:c.5050C>T	ENSP00000496981.1:p.Pro1684Ser
ENST00000281928.7:c.5050C>T	ENSP00000281928.3:p.Pro1684Ser
ENST00000549786.1:c.414C>T
ENST00000552340.1:c.82C>T	ENSP00000449876.1:p.Pro28Ser
NM_015335.4:c.5050C>T	NP_056150.1:p.Pro1684Ser
XM_011538080.1:c.5050C>T	XP_011536382.1:p.Pro1684Ser
XM_011538081.1:c.5047C>T	XP_011536383.1:p.Pro1683Ser
XM_011538082.1:c.5020C>T	XP_011536384.1:p.Pro1674Ser
XM_011538080.2:c.5050C>T	XP_011536382.1:p.Pro1684Ser
XM_011538081.2:c.5047C>T	XP_011536383.1:p.Pro1683Ser
XM_011538082.2:c.5020C>T	XP_011536384.1:p.Pro1674Ser
XM_017019090.1:c.5047C>T	XP_016874579.1:p.Pro1683Ser
NM_015335.5:c.5050C>T MANE Select	NP_056150.1:p.Pro1684Ser