Canonical Allele Identifier: CA1202313652

Gene: VANGL2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160424991_160424992delinsGT , CM000663.2:g.160424991_160424992delinsGT	GRCh38
NC_000001.10:g.160394781_160394782delinsGT , CM000663.1:g.160394781_160394782delinsGT	GRCh37
NC_000001.9:g.158661405_158661406delinsGT	NCBI36
NG_023420.1:g.29418_29419delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696602.1:c.1450-127_1450-126delinsGT	ENSP00000512747.1:n.1450-127_1450-126delinsGT
ENST00000368061.3:c.1306-127_1306-126delinsGT MANE Select	ENSP00000357040.2:n.1306-127_1306-126delinsGT
ENST00000368061.2:c.1306-127_1306-126delinsGT	ENSP00000357040.2:n.1306-127_1306-126delinsGT
NM_020335.2:c.1306-127_1306-126delinsGT	NP_065068.1:n.1306-127_1306-126delinsGT
XM_005245357.1:c.1306-127_1306-126delinsGT	XP_005245414.1:n.1306-127_1306-126delinsGT
XM_011509804.1:c.1306-127_1306-126delinsGT	XP_011508106.1:n.1306-127_1306-126delinsGT
NM_020335.3:c.1306-127_1306-126delinsGT MANE Select	NP_065068.1:n.1306-127_1306-126delinsGT