Canonical Allele Identifier: CA476145138

Linked Data

MyVariant Identifiers: chr11:g.86663369C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952327C>T , CM000673.2:g.86952327C>T GRCh38
NC_000011.9:g.86663369C>T , CM000673.1:g.86663369C>T GRCh37
NC_000011.8:g.86341017C>T NCBI36
NG_011752.1:g.8065G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.429G>A (FZD4) MANE Select ENSP00000434034.1:p.Leu143=
ENST00000531380.1:c.429G>A (FZD4) ENSP00000434034.1:p.Leu143=
ENST00000532234.5:c.*1320C>T (PRSS23) ENSP00000436676.1:n.*1320C>T
ENST00000533902.2:c.*1042C>T (PRSS23) ENSP00000437268.1:n.*1042C>T
NM_012193.3:c.429G>A (FZD4) NP_036325.2:p.Leu143=
NR_120591.1:n.1992C>T (PRSS23)
NR_120592.1:n.1741C>T (PRSS23)
NR_120591.2:n.1690C>T (PRSS23)
NR_120592.2:n.1439C>T (PRSS23)
NM_012193.4:c.429G>A (FZD4) MANE Select NP_036325.2:p.Leu143=
NR_120591.3:n.1690C>T (PRSS23)