Canonical Allele Identifier: CA2797588529

Gene: MED13L

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115996773_115996774insCACACCCAAC , CM000674.2:g.115996773_115996774insCACACCCAAC	GRCh38
NC_000012.11:g.116434578_116434579insCACACCCAAC , CM000674.1:g.116434578_116434579insCACACCCAAC	GRCh37
NC_000012.10:g.114918961_114918962insCACACCCAAC	NCBI36
NG_023366.1:g.285413_285414insGTTGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2791-93_2791-92insGTTGGGTGTG MANE Select	ENSP00000281928.3:n.2791-93_2791-92insGTTGGGTGTG
ENST00000548743.2:c.2761-93_2761-92insGTTGGGTGTG	ENSP00000448553.2:n.2761-93_2761-92insGTTGGGTGTG
ENST00000549786.2:c.2219-93_2219-92insGTTGGGTGTG
ENST00000647927.1:n.3164-93_3164-92insGTTGGGTGTG
ENST00000648173.1:n.1586-93_1586-92insGTTGGGTGTG
ENST00000648379.1:n.1159-93_1159-92insGTTGGGTGTG
ENST00000648737.1:n.2555-93_2555-92insGTTGGGTGTG
ENST00000648916.1:n.802-93_802-92insGTTGGGTGTG
ENST00000649607.1:c.975-93_975-92insGTTGGGTGTG
ENST00000650226.1:c.2791-93_2791-92insGTTGGGTGTG	ENSP00000496981.1:n.2791-93_2791-92insGTTGGGTGTG
ENST00000281928.7:c.2791-93_2791-92insGTTGGGTGTG	ENSP00000281928.3:n.2791-93_2791-92insGTTGGGTGTG
NM_015335.4:c.2791-93_2791-92insGTTGGGTGTG	NP_056150.1:n.2791-93_2791-92insGTTGGGTGTG
XM_011538080.1:c.2791-93_2791-92insGTTGGGTGTG	XP_011536382.1:n.2791-93_2791-92insGTTGGGTGTG
XM_011538081.1:c.2788-93_2788-92insGTTGGGTGTG	XP_011536383.1:n.2788-93_2788-92insGTTGGGTGTG
XM_011538082.1:c.2761-93_2761-92insGTTGGGTGTG	XP_011536384.1:n.2761-93_2761-92insGTTGGGTGTG
XM_011538080.2:c.2791-93_2791-92insGTTGGGTGTG	XP_011536382.1:n.2791-93_2791-92insGTTGGGTGTG
XM_011538081.2:c.2788-93_2788-92insGTTGGGTGTG	XP_011536383.1:n.2788-93_2788-92insGTTGGGTGTG
XM_011538082.2:c.2761-93_2761-92insGTTGGGTGTG	XP_011536384.1:n.2761-93_2761-92insGTTGGGTGTG
XM_017019090.1:c.2788-93_2788-92insGTTGGGTGTG	XP_016874579.1:n.2788-93_2788-92insGTTGGGTGTG
NM_015335.5:c.2791-93_2791-92insGTTGGGTGTG MANE Select	NP_056150.1:n.2791-93_2791-92insGTTGGGTGTG