Canonical Allele Identifier: CA386882328

Gene: MED13L

Linked Data

• gnomAD v4: 12-115982599-T-A
• MyVariant Identifiers: chr12:g.116420404T>A (hg19) ; chr12:g.115982599T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115982599T>A , CM000674.2:g.115982599T>A	GRCh38
NC_000012.11:g.116420404T>A , CM000674.1:g.116420404T>A	GRCh37
NC_000012.10:g.114904787T>A	NCBI36
NG_023366.1:g.299588A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.4960A>T MANE Select	ENSP00000281928.3:p.Thr1654Ser
ENST00000549786.2:c.4388A>T
ENST00000648379.1:n.3328A>T
ENST00000648737.1:n.4724A>T
ENST00000648825.1:n.1700A>T
ENST00000648916.1:n.2971A>T
ENST00000649146.1:n.2203A>T
ENST00000649607.1:c.3144A>T
ENST00000649775.1:c.1453-4A>T
ENST00000650226.1:c.4960A>T	ENSP00000496981.1:p.Thr1654Ser
ENST00000281928.7:c.4960A>T	ENSP00000281928.3:p.Thr1654Ser
ENST00000549786.1:c.324A>T
NM_015335.4:c.4960A>T	NP_056150.1:p.Thr1654Ser
XM_011538080.1:c.4960A>T	XP_011536382.1:p.Thr1654Ser
XM_011538081.1:c.4957A>T	XP_011536383.1:p.Thr1653Ser
XM_011538082.1:c.4930A>T	XP_011536384.1:p.Thr1644Ser
XM_011538080.2:c.4960A>T	XP_011536382.1:p.Thr1654Ser
XM_011538081.2:c.4957A>T	XP_011536383.1:p.Thr1653Ser
XM_011538082.2:c.4930A>T	XP_011536384.1:p.Thr1644Ser
XM_017019090.1:c.4957A>T	XP_016874579.1:p.Thr1653Ser
NM_015335.5:c.4960A>T MANE Select	NP_056150.1:p.Thr1654Ser