Canonical Allele Identifier: CA476144771

Linked Data

MyVariant Identifiers: chr11:g.86662853G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951811G>T , CM000673.2:g.86951811G>T GRCh38
NC_000011.9:g.86662853G>T , CM000673.1:g.86662853G>T GRCh37
NC_000011.8:g.86340501G>T NCBI36
NG_011752.1:g.8581C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.945C>A (FZD4) MANE Select ENSP00000434034.1:p.Ala315=
ENST00000531380.1:c.945C>A (FZD4) ENSP00000434034.1:p.Ala315=
ENST00000532234.5:c.*804G>T (PRSS23) ENSP00000436676.1:n.*804G>T
ENST00000533902.2:c.*526G>T (PRSS23) ENSP00000437268.1:n.*526G>T
NM_012193.3:c.945C>A (FZD4) NP_036325.2:p.Ala315=
NR_120591.1:n.1476G>T (PRSS23)
NR_120592.1:n.1225G>T (PRSS23)
NR_120591.2:n.1174G>T (PRSS23)
NR_120592.2:n.923G>T (PRSS23)
NM_012193.4:c.945C>A (FZD4) MANE Select NP_036325.2:p.Ala315=
NR_120591.3:n.1174G>T (PRSS23)