Canonical Allele Identifier: CA476145135

Linked Data

MyVariant Identifiers: chr11:g.86663366G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952324G>A , CM000673.2:g.86952324G>A GRCh38
NC_000011.9:g.86663366G>A , CM000673.1:g.86663366G>A GRCh37
NC_000011.8:g.86341014G>A NCBI36
NG_011752.1:g.8068C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.432C>T (FZD4) MANE Select ENSP00000434034.1:p.Asn144=
ENST00000531380.1:c.432C>T (FZD4) ENSP00000434034.1:p.Asn144=
ENST00000532234.5:c.*1317G>A (PRSS23) ENSP00000436676.1:n.*1317G>A
ENST00000533902.2:c.*1039G>A (PRSS23) ENSP00000437268.1:n.*1039G>A
NM_012193.3:c.432C>T (FZD4) NP_036325.2:p.Asn144=
NR_120591.1:n.1989G>A (PRSS23)
NR_120592.1:n.1738G>A (PRSS23)
NR_120591.2:n.1687G>A (PRSS23)
NR_120592.2:n.1436G>A (PRSS23)
NM_012193.4:c.432C>T (FZD4) MANE Select NP_036325.2:p.Asn144=
NR_120591.3:n.1687G>A (PRSS23)