Canonical Allele Identifier: CA481951160

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116450685T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116012880T>A , CM000674.2:g.116012880T>A	GRCh38
NC_000012.11:g.116450685T>A , CM000674.1:g.116450685T>A	GRCh37
NC_000012.10:g.114935068T>A	NCBI36
NG_023366.1:g.269307A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.1197A>T MANE Select	ENSP00000281928.3:p.Pro399=
ENST00000548743.2:c.1167A>T	ENSP00000448553.2:p.Pro389=
ENST00000549786.2:c.625A>T
ENST00000647567.1:c.1104A>T	ENSP00000497136.1:p.Pro368=
ENST00000648737.1:n.961A>T
ENST00000650226.1:c.1197A>T	ENSP00000496981.1:p.Pro399=
ENST00000281928.7:c.1197A>T	ENSP00000281928.3:p.Pro399=
NM_015335.4:c.1197A>T	NP_056150.1:p.Pro399=
XM_011538080.1:c.1197A>T	XP_011536382.1:p.Pro399=
XM_011538081.1:c.1197A>T	XP_011536383.1:p.Pro399=
XM_011538082.1:c.1167A>T	XP_011536384.1:p.Pro389=
XM_011538080.2:c.1197A>T	XP_011536382.1:p.Pro399=
XM_011538081.2:c.1197A>T	XP_011536383.1:p.Pro399=
XM_011538082.2:c.1167A>T	XP_011536384.1:p.Pro389=
XM_017019090.1:c.1197A>T	XP_016874579.1:p.Pro399=
NM_015335.5:c.1197A>T MANE Select	NP_056150.1:p.Pro399=