Canonical Allele Identifier: CA481949677

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116435025G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997220G>A , CM000674.2:g.115997220G>A	GRCh38
NC_000012.11:g.116435025G>A , CM000674.1:g.116435025G>A	GRCh37
NC_000012.10:g.114919408G>A	NCBI36
NG_023366.1:g.284967C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2580C>T MANE Select	ENSP00000281928.3:p.Asp860=
ENST00000548743.2:c.2550C>T	ENSP00000448553.2:p.Asp850=
ENST00000549786.2:c.2008C>T
ENST00000647927.1:n.2953C>T
ENST00000648173.1:n.1375C>T
ENST00000648379.1:n.948C>T
ENST00000648737.1:n.2344C>T
ENST00000648916.1:n.591C>T
ENST00000649607.1:c.764C>T
ENST00000650226.1:c.2580C>T	ENSP00000496981.1:p.Asp860=
ENST00000281928.7:c.2580C>T	ENSP00000281928.3:p.Asp860=
NM_015335.4:c.2580C>T	NP_056150.1:p.Asp860=
XM_011538080.1:c.2580C>T	XP_011536382.1:p.Asp860=
XM_011538081.1:c.2577C>T	XP_011536383.1:p.Asp859=
XM_011538082.1:c.2550C>T	XP_011536384.1:p.Asp850=
XM_011538080.2:c.2580C>T	XP_011536382.1:p.Asp860=
XM_011538081.2:c.2577C>T	XP_011536383.1:p.Asp859=
XM_011538082.2:c.2550C>T	XP_011536384.1:p.Asp850=
XM_017019090.1:c.2577C>T	XP_016874579.1:p.Asp859=
NM_015335.5:c.2580C>T MANE Select	NP_056150.1:p.Asp860=