Canonical Allele Identifier: CA481949986

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116440809T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116003004T>A , CM000674.2:g.116003004T>A	GRCh38
NC_000012.11:g.116440809T>A , CM000674.1:g.116440809T>A	GRCh37
NC_000012.10:g.114925192T>A	NCBI36
NG_023366.1:g.279183A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2568A>T MANE Select	ENSP00000281928.3:p.Pro856=
ENST00000548743.2:c.2538A>T	ENSP00000448553.2:p.Pro846=
ENST00000549786.2:c.1996A>T
ENST00000648173.1:n.1363A>T
ENST00000648379.1:n.936A>T
ENST00000648737.1:n.2332A>T
ENST00000648916.1:n.579A>T
ENST00000649607.1:c.755A>T
ENST00000650226.1:c.2568A>T	ENSP00000496981.1:p.Pro856=
ENST00000281928.7:c.2568A>T	ENSP00000281928.3:p.Pro856=
NM_015335.4:c.2568A>T	NP_056150.1:p.Pro856=
XM_011538080.1:c.2568A>T	XP_011536382.1:p.Pro856=
XM_011538081.1:c.2568A>T	XP_011536383.1:p.Pro856=
XM_011538082.1:c.2538A>T	XP_011536384.1:p.Pro846=
XM_011538080.2:c.2568A>T	XP_011536382.1:p.Pro856=
XM_011538081.2:c.2568A>T	XP_011536383.1:p.Pro856=
XM_011538082.2:c.2538A>T	XP_011536384.1:p.Pro846=
XM_017019090.1:c.2568A>T	XP_016874579.1:p.Pro856=
NM_015335.5:c.2568A>T MANE Select	NP_056150.1:p.Pro856=