Canonical Allele Identifier: CA386881400

Gene: MED13L

Linked Data

• gnomAD v4: 12-115982566-G-A
• MyVariant Identifiers: chr12:g.116420371G>A (hg19) ; chr12:g.115982566G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982566G>A , CM000674.2:g.115982566G>A	GRCh38
NC_000012.11:g.116420371G>A , CM000674.1:g.116420371G>A	GRCh37
NC_000012.10:g.114904754G>A	NCBI36
NG_023366.1:g.299621C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4993C>T MANE Select	ENSP00000281928.3:p.Pro1665Ser
ENST00000549786.2:c.4421C>T
ENST00000648379.1:n.3361C>T
ENST00000648737.1:n.4757C>T
ENST00000648825.1:n.1733C>T
ENST00000648916.1:n.3004C>T
ENST00000649146.1:n.2236C>T
ENST00000649607.1:c.3177C>T
ENST00000649775.1:c.1482C>T
ENST00000650226.1:c.4993C>T	ENSP00000496981.1:p.Pro1665Ser
ENST00000281928.7:c.4993C>T	ENSP00000281928.3:p.Pro1665Ser
ENST00000549786.1:c.357C>T
ENST00000552340.1:c.25C>T	ENSP00000449876.1:p.Pro9Ser
NM_015335.4:c.4993C>T	NP_056150.1:p.Pro1665Ser
XM_011538080.1:c.4993C>T	XP_011536382.1:p.Pro1665Ser
XM_011538081.1:c.4990C>T	XP_011536383.1:p.Pro1664Ser
XM_011538082.1:c.4963C>T	XP_011536384.1:p.Pro1655Ser
XM_011538080.2:c.4993C>T	XP_011536382.1:p.Pro1665Ser
XM_011538081.2:c.4990C>T	XP_011536383.1:p.Pro1664Ser
XM_011538082.2:c.4963C>T	XP_011536384.1:p.Pro1655Ser
XM_017019090.1:c.4990C>T	XP_016874579.1:p.Pro1664Ser
NM_015335.5:c.4993C>T MANE Select	NP_056150.1:p.Pro1665Ser