Canonical Allele Identifier: CA2578563056

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923260_30923269del , CM000668.2:g.30923260_30923269del	GRCh38
NC_000006.11:g.30891037_30891046del , CM000668.1:g.30891037_30891046del	GRCh37
NC_000006.10:g.30999016_30999025del	NCBI36
NG_034224.1:g.14053_14062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2313+29_2313+38del	ENSP00000441000.2:n.2313+29_2313+38del
ENST00000672801.1:c.2307+29_2307+38del	ENSP00000500615.1:n.2307+29_2307+38del
ENST00000676266.1:c.2313+29_2313+38del MANE Select	ENSP00000502585.1:n.2313+29_2313+38del
ENST00000321897.9:c.2313+29_2313+38del	ENSP00000316092.5:n.2313+29_2313+38del
ENST00000469358.5:n.2301+29_2301+38del
ENST00000473916.1:n.24+29_24+38del
ENST00000476162.5:n.1100+29_1100+38del
ENST00000477052.1:n.399+29_399+38del
ENST00000477288.5:n.4926+29_4926+38del
ENST00000541562.5:c.2403+29_2403+38del	ENSP00000441000.1:n.2403+29_2403+38del
ENST00000542001.5:c.2307+29_2307+38del	ENSP00000438200.2:n.2307+29_2307+38del
ENST00000625423.2:c.1893+29_1893+38del	ENSP00000485818.1:n.1893+29_1893+38del
NM_001167733.2:c.1893+29_1893+38del	NP_001161205.1:n.1893+29_1893+38del
NM_001167734.1:c.2403+29_2403+38del	NP_001161206.1:n.2403+29_2403+38del
NM_020442.5:c.2313+29_2313+38del	NP_065175.4:n.2313+29_2313+38del
NM_001167733.3:c.1893+29_1893+38del	NP_001161205.1:n.1893+29_1893+38del
NM_001167734.2:c.2403+29_2403+38del	NP_001161206.1:n.2403+29_2403+38del
NM_020442.6:c.2313+29_2313+38del MANE Select	NP_065175.4:n.2313+29_2313+38del