Canonical Allele Identifier: CA1023575
Community Standard Title: NM_138959.3(VANGL1):c.*25A>T
Gene: VANGL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115691404A>T , CM000663.2:g.115691404A>T GRCh38
NC_000001.10:g.116234025A>T , CM000663.1:g.116234025A>T GRCh37
NC_000001.9:g.116035548A>T NCBI36
NG_016548.1:g.54452A>T

Transcript Alleles

HGVS Amino-acid Change
NM_138959.3:c.*25A>T MANE Select NP_620409.1:n.*25A>T
ENST00000355485.7:c.*25A>T MANE Select ENSP00000347672.2:n.*25A>T
NM_001172411.1:c.*25A>T NP_001165882.1:n.*25A>T
NM_001172411.2:c.*25A>T NP_001165882.1:n.*25A>T
NM_001172412.1:c.*25A>T NP_001165883.1:n.*25A>T
NM_001172412.2:c.*25A>T NP_001165883.1:n.*25A>T
NM_138959.2:c.*25A>T NP_620409.1:n.*25A>T
ENST00000310260.7:c.*25A>T ENSP00000310800.3:n.*25A>T
ENST00000355485.6:c.*25A>T ENSP00000347672.2:n.*25A>T
ENST00000369509.1:c.*25A>T ENSP00000358522.1:n.*25A>T
ENST00000369510.8:c.*25A>T ENSP00000358523.3:n.*25A>T