Canonical Allele Identifier: CA2513789914

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922882_30922883insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC , CM000668.2:g.30922882_30922883insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	GRCh38
NC_000006.11:g.30890659_30890660insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC , CM000668.1:g.30890659_30890660insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	GRCh37
NC_000006.10:g.30998638_30998639insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	NCBI36
NG_034224.1:g.13675_13676insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2107-16_2107-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	ENSP00000441000.2:n.2107-16_2107-15insACCATTGGTGATTTCGCTTTCGG...
ENST00000672801.1:c.2101-16_2101-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	ENSP00000500615.1:n.2101-16_2101-15insACCATTGGTGATTTCGCTTTCGG...
ENST00000676266.1:c.2107-16_2107-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC MANE Select	ENSP00000502585.1:n.2107-16_2107-15insACCATTGGTGATTTCGCTTTCGG...
ENST00000321897.9:c.2107-16_2107-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	ENSP00000316092.5:n.2107-16_2107-15insACCATTGGTGATTTCGCTTTCGG...
ENST00000469358.5:n.2095-16_2095-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC
ENST00000476162.5:n.894-16_894-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC
ENST00000477052.1:n.193-16_193-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC
ENST00000477288.5:n.4720-16_4720-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC
ENST00000541562.5:c.2197-16_2197-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	ENSP00000441000.1:n.2197-16_2197-15insACCATTGGTGATTTCGCTTTCGG...
ENST00000542001.5:c.2101-16_2101-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	ENSP00000438200.2:n.2101-16_2101-15insACCATTGGTGATTTCGCTTTCGG...
ENST00000625423.2:c.1687-16_1687-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	ENSP00000485818.1:n.1687-16_1687-15insACCATTGGTGATTTCGCTTTCGG...
NM_001167733.2:c.1687-16_1687-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	NP_001161205.1:n.1687-16_1687-15insACCATTGGTGATTTCGCTTTCGGTAA...
NM_001167734.1:c.2197-16_2197-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	NP_001161206.1:n.2197-16_2197-15insACCATTGGTGATTTCGCTTTCGGTAA...
NM_020442.5:c.2107-16_2107-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	NP_065175.4:n.2107-16_2107-15insACCATTGGTGATTTCGCTTTCGGTAAGCA...
NM_001167733.3:c.1687-16_1687-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	NP_001161205.1:n.1687-16_1687-15insACCATTGGTGATTTCGCTTTCGGTAA...
NM_001167734.2:c.2197-16_2197-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC	NP_001161206.1:n.2197-16_2197-15insACCATTGGTGATTTCGCTTTCGGTAA...
NM_020442.6:c.2107-16_2107-15insACCATTGGTGATTTCGCTTTCGGTAAGCAGAACGTACTGATTCTGCTGTCCGTGGTGATTAGCGCGGTCTTC MANE Select	NP_065175.4:n.2107-16_2107-15insACCATTGGTGATTTCGCTTTCGGTAAGCA...