Canonical Allele Identifier: CA482137374

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429306A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991501A>G , CM000674.2:g.115991501A>G	GRCh38
NC_000012.11:g.116429306A>G , CM000674.1:g.116429306A>G	GRCh37
NC_000012.10:g.114913689A>G	NCBI36
NG_023366.1:g.290686T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3453T>C MANE Select	ENSP00000281928.3:p.Asp1151=
ENST00000549786.2:c.2881T>C
ENST00000648379.1:n.1821T>C
ENST00000648737.1:n.3217T>C
ENST00000648825.1:n.193T>C
ENST00000648916.1:n.1464T>C
ENST00000649607.1:c.1637T>C
ENST00000650226.1:c.3453T>C	ENSP00000496981.1:p.Asp1151=
ENST00000281928.7:c.3453T>C	ENSP00000281928.3:p.Asp1151=
NM_015335.4:c.3453T>C	NP_056150.1:p.Asp1151=
XM_011538080.1:c.3453T>C	XP_011536382.1:p.Asp1151=
XM_011538081.1:c.3450T>C	XP_011536383.1:p.Asp1150=
XM_011538082.1:c.3423T>C	XP_011536384.1:p.Asp1141=
XM_011538080.2:c.3453T>C	XP_011536382.1:p.Asp1151=
XM_011538081.2:c.3450T>C	XP_011536383.1:p.Asp1150=
XM_011538082.2:c.3423T>C	XP_011536384.1:p.Asp1141=
XM_017019090.1:c.3450T>C	XP_016874579.1:p.Asp1150=
NM_015335.5:c.3453T>C MANE Select	NP_056150.1:p.Asp1151=