Canonical Allele Identifier: CA476144483

Linked Data

MyVariant Identifiers: chr11:g.86662640G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951598G>C , CM000673.2:g.86951598G>C GRCh38
NC_000011.9:g.86662640G>C , CM000673.1:g.86662640G>C GRCh37
NC_000011.8:g.86340288G>C NCBI36
NG_011752.1:g.8794C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1158C>G (FZD4) MANE Select ENSP00000434034.1:p.Ala386=
ENST00000531380.1:c.1158C>G (FZD4) ENSP00000434034.1:p.Ala386=
ENST00000531521.1:n.769G>C (PRSS23)
ENST00000532234.5:c.*591G>C (PRSS23) ENSP00000436676.1:n.*591G>C
ENST00000533902.2:c.*313G>C (PRSS23) ENSP00000437268.1:n.*313G>C
NM_012193.3:c.1158C>G (FZD4) NP_036325.2:p.Ala386=
NR_120591.1:n.1263G>C (PRSS23)
NR_120592.1:n.1012G>C (PRSS23)
NR_120591.2:n.961G>C (PRSS23)
NR_120592.2:n.710G>C (PRSS23)
NM_012193.4:c.1158C>G (FZD4) MANE Select NP_036325.2:p.Ala386=
NR_120591.3:n.961G>C (PRSS23)