Canonical Allele Identifier: CA1023411
Community Standard Title: NM_138959.3(VANGL1):c.1023C>T (p.Asn341=)
Gene: VANGL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115684020C>T , CM000663.2:g.115684020C>T GRCh38
NC_000001.10:g.116226641C>T , CM000663.1:g.116226641C>T GRCh37
NC_000001.9:g.116028164C>T NCBI36
NG_016548.1:g.47068C>T

Transcript Alleles

HGVS Amino-acid Change
NM_138959.3:c.1023C>T MANE Select NP_620409.1:p.Asn341=
ENST00000355485.7:c.1023C>T MANE Select ENSP00000347672.2:p.Asn341=
NM_001172411.1:c.1017C>T NP_001165882.1:p.Asn339=
NM_001172411.2:c.1017C>T NP_001165882.1:p.Asn339=
NM_001172412.1:c.1023C>T NP_001165883.1:p.Asn341=
NM_001172412.2:c.1023C>T NP_001165883.1:p.Asn341=
NM_138959.2:c.1023C>T NP_620409.1:p.Asn341=
ENST00000310260.7:c.1023C>T ENSP00000310800.3:p.Asn341=
ENST00000355485.6:c.1023C>T ENSP00000347672.2:p.Asn341=
ENST00000369509.1:c.1023C>T ENSP00000358522.1:p.Asn341=
ENST00000369510.8:c.1017C>T ENSP00000358523.3:p.Asn339=
ENST00000474344.1:n.405C>T
ENST00000478369.5:n.307C>T