Canonical Allele Identifier: CA482137387

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429579G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991774G>T , CM000674.2:g.115991774G>T	GRCh38
NC_000012.11:g.116429579G>T , CM000674.1:g.116429579G>T	GRCh37
NC_000012.10:g.114913962G>T	NCBI36
NG_023366.1:g.290413C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3180C>A MANE Select	ENSP00000281928.3:p.Pro1060=
ENST00000548743.2:c.3150C>A	ENSP00000448553.2:p.Pro1050=
ENST00000549786.2:c.2608C>A
ENST00000648173.1:n.1975C>A
ENST00000648379.1:n.1548C>A
ENST00000648737.1:n.2944C>A
ENST00000648916.1:n.1191C>A
ENST00000649607.1:c.1364C>A
ENST00000650226.1:c.3180C>A	ENSP00000496981.1:p.Pro1060=
ENST00000281928.7:c.3180C>A	ENSP00000281928.3:p.Pro1060=
NM_015335.4:c.3180C>A	NP_056150.1:p.Pro1060=
XM_011538080.1:c.3180C>A	XP_011536382.1:p.Pro1060=
XM_011538081.1:c.3177C>A	XP_011536383.1:p.Pro1059=
XM_011538082.1:c.3150C>A	XP_011536384.1:p.Pro1050=
XM_011538080.2:c.3180C>A	XP_011536382.1:p.Pro1060=
XM_011538081.2:c.3177C>A	XP_011536383.1:p.Pro1059=
XM_011538082.2:c.3150C>A	XP_011536384.1:p.Pro1050=
XM_017019090.1:c.3177C>A	XP_016874579.1:p.Pro1059=
NM_015335.5:c.3180C>A MANE Select	NP_056150.1:p.Pro1060=