Canonical Allele Identifier: CA1202313689
Gene: VANGL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425048A= , CM000663.2:g.160425048A= GRCh38
NC_000001.10:g.160394838A= , CM000663.1:g.160394838A= GRCh37
NC_000001.9:g.158661462A= NCBI36
NG_023420.1:g.29475A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-70A= ENSP00000512747.1:n.1450-70A=
ENST00000368061.3:c.1306-70A= MANE Select ENSP00000357040.2:n.1306-70A=
ENST00000368061.2:c.1306-70A= ENSP00000357040.2:n.1306-70A=
NM_020335.2:c.1306-70A= NP_065068.1:n.1306-70A=
XM_005245357.1:c.1306-70A= XP_005245414.1:n.1306-70A=
XM_011509804.1:c.1306-70A= XP_011508106.1:n.1306-70A=
NM_020335.3:c.1306-70A= MANE Select NP_065068.1:n.1306-70A=
Search 100 bp 5'
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