Canonical Allele Identifier: CA482137208

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429450A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991645A>G , CM000674.2:g.115991645A>G	GRCh38
NC_000012.11:g.116429450A>G , CM000674.1:g.116429450A>G	GRCh37
NC_000012.10:g.114913833A>G	NCBI36
NG_023366.1:g.290542T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3309T>C MANE Select	ENSP00000281928.3:p.Ile1103=
ENST00000549786.2:c.2737T>C
ENST00000648379.1:n.1677T>C
ENST00000648737.1:n.3073T>C
ENST00000648825.1:n.49T>C
ENST00000648916.1:n.1320T>C
ENST00000649607.1:c.1493T>C
ENST00000650226.1:c.3309T>C	ENSP00000496981.1:p.Ile1103=
ENST00000281928.7:c.3309T>C	ENSP00000281928.3:p.Ile1103=
NM_015335.4:c.3309T>C	NP_056150.1:p.Ile1103=
XM_011538080.1:c.3309T>C	XP_011536382.1:p.Ile1103=
XM_011538081.1:c.3306T>C	XP_011536383.1:p.Ile1102=
XM_011538082.1:c.3279T>C	XP_011536384.1:p.Ile1093=
XM_011538080.2:c.3309T>C	XP_011536382.1:p.Ile1103=
XM_011538081.2:c.3306T>C	XP_011536383.1:p.Ile1102=
XM_011538082.2:c.3279T>C	XP_011536384.1:p.Ile1093=
XM_017019090.1:c.3306T>C	XP_016874579.1:p.Ile1102=
NM_015335.5:c.3309T>C MANE Select	NP_056150.1:p.Ile1103=