Canonical Allele Identifier: CA1618928448

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923110_30923111delinsAC , CM000668.2:g.30923110_30923111delinsAC	GRCh38
NC_000006.11:g.30890887_30890888delinsAC , CM000668.1:g.30890887_30890888delinsAC	GRCh37
NC_000006.10:g.30998866_30998867delinsAC	NCBI36
NG_034224.1:g.13903_13904delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2192_2193delinsAC	ENSP00000441000.2:p.Asp731=
ENST00000672801.1:c.2186_2187delinsAC	ENSP00000500615.1:p.Asp729=
ENST00000676266.1:c.2192_2193delinsAC MANE Select	ENSP00000502585.1:p.Asp731=
ENST00000321897.9:c.2192_2193delinsAC	ENSP00000316092.5:p.Asp731=
ENST00000469358.5:n.2180_2181delinsAC
ENST00000476162.5:n.979_980delinsAC
ENST00000477052.1:n.278_279delinsAC
ENST00000477288.5:n.4805_4806delinsAC
ENST00000541562.5:c.2282_2283delinsAC	ENSP00000441000.1:p.Asp761=
ENST00000542001.5:c.2186_2187delinsAC	ENSP00000438200.2:p.Asp729=
ENST00000625423.2:c.1772_1773delinsAC	ENSP00000485818.1:p.Asp591=
NM_001167733.2:c.1772_1773delinsAC	NP_001161205.1:p.Asp591=
NM_001167734.1:c.2282_2283delinsAC	NP_001161206.1:p.Asp761=
NM_020442.5:c.2192_2193delinsAC	NP_065175.4:p.Asp731=
NM_001167733.3:c.1772_1773delinsAC	NP_001161205.1:p.Asp591=
NM_001167734.2:c.2282_2283delinsAC	NP_001161206.1:p.Asp761=
NM_020442.6:c.2192_2193delinsAC MANE Select	NP_065175.4:p.Asp731=