Canonical Allele Identifier: CA2544594647

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116012735_116012736insTTCG , CM000674.2:g.116012735_116012736insTTCG	GRCh38
NC_000012.11:g.116450540_116450541insTTCG , CM000674.1:g.116450540_116450541insTTCG	GRCh37
NC_000012.10:g.114934923_114934924insTTCG	NCBI36
NG_023366.1:g.269452_269453insGAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.1280+62_1280+63insGAAC MANE Select	ENSP00000281928.3:n.1280+62_1280+63insGAAC
ENST00000548743.2:c.1250+62_1250+63insGAAC	ENSP00000448553.2:n.1250+62_1250+63insGAAC
ENST00000549786.2:c.708+62_708+63insGAAC
ENST00000647567.1:c.1187+62_1187+63insGAAC	ENSP00000497136.1:n.1187+62_1187+63insGAAC
ENST00000648737.1:n.1044+62_1044+63insGAAC
ENST00000650226.1:c.1280+62_1280+63insGAAC	ENSP00000496981.1:n.1280+62_1280+63insGAAC
ENST00000281928.7:c.1280+62_1280+63insGAAC	ENSP00000281928.3:n.1280+62_1280+63insGAAC
NM_015335.4:c.1280+62_1280+63insGAAC	NP_056150.1:n.1280+62_1280+63insGAAC
XM_011538080.1:c.1280+62_1280+63insGAAC	XP_011536382.1:n.1280+62_1280+63insGAAC
XM_011538081.1:c.1280+62_1280+63insGAAC	XP_011536383.1:n.1280+62_1280+63insGAAC
XM_011538082.1:c.1250+62_1250+63insGAAC	XP_011536384.1:n.1250+62_1250+63insGAAC
XM_011538080.2:c.1280+62_1280+63insGAAC	XP_011536382.1:n.1280+62_1280+63insGAAC
XM_011538081.2:c.1280+62_1280+63insGAAC	XP_011536383.1:n.1280+62_1280+63insGAAC
XM_011538082.2:c.1250+62_1250+63insGAAC	XP_011536384.1:n.1250+62_1250+63insGAAC
XM_017019090.1:c.1280+62_1280+63insGAAC	XP_016874579.1:n.1280+62_1280+63insGAAC
NM_015335.5:c.1280+62_1280+63insGAAC MANE Select	NP_056150.1:n.1280+62_1280+63insGAAC