Canonical Allele Identifier: CA1202313625
Gene: VANGL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160424947T= , CM000663.2:g.160424947T= GRCh38
NC_000001.10:g.160394737T= , CM000663.1:g.160394737T= GRCh37
NC_000001.9:g.158661361T= NCBI36
NG_023420.1:g.29374T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-171T= ENSP00000512747.1:n.1450-171T=
ENST00000368061.3:c.1306-171T= MANE Select ENSP00000357040.2:n.1306-171T=
ENST00000368061.2:c.1306-171T= ENSP00000357040.2:n.1306-171T=
NM_020335.2:c.1306-171T= NP_065068.1:n.1306-171T=
XM_005245357.1:c.1306-171T= XP_005245414.1:n.1306-171T=
XM_011509804.1:c.1306-171T= XP_011508106.1:n.1306-171T=
NM_020335.3:c.1306-171T= MANE Select NP_065068.1:n.1306-171T=
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