Canonical Allele Identifier: CA2575306865

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116012901_116012903del , CM000674.2:g.116012901_116012903del	GRCh38
NC_000012.11:g.116450706_116450708del , CM000674.1:g.116450706_116450708del	GRCh37
NC_000012.10:g.114935089_114935091del	NCBI36
NG_023366.1:g.269289_269291del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.1179_1181del
ENST00000548743.2:c.1149_1151del
ENST00000549786.2:c.607_609del
ENST00000647567.1:c.1086_1088del
ENST00000648737.1:n.943_945del
ENST00000650226.1:c.1179_1181del
ENST00000281928.7:c.1179_1181del
NM_015335.4:c.1179_1181del
XM_011538080.1:c.1179_1181del
XM_011538081.1:c.1179_1181del
XM_011538082.1:c.1149_1151del
XM_011538080.2:c.1179_1181del
XM_011538081.2:c.1179_1181del
XM_011538082.2:c.1149_1151del
XM_017019090.1:c.1179_1181del
NM_015335.5:c.1179_1181del