Canonical Allele Identifier: CA382015578

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952188G>T , CM000673.2:g.86952188G>T GRCh38
NC_000011.9:g.86663230G>T , CM000673.1:g.86663230G>T GRCh37
NC_000011.8:g.86340878G>T NCBI36
NG_011752.1:g.8204C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.568C>A (FZD4) MANE Select ENSP00000434034.1:p.Gln190Lys
ENST00000531380.1:c.568C>A (FZD4) ENSP00000434034.1:p.Gln190Lys
ENST00000532234.5:c.*1181G>T (PRSS23) ENSP00000436676.1:n.*1181G>T
ENST00000533902.2:c.*903G>T (PRSS23) ENSP00000437268.1:n.*903G>T
NM_012193.3:c.568C>A (FZD4) NP_036325.2:p.Gln190Lys
NR_120591.1:n.1853G>T (PRSS23)
NR_120592.1:n.1602G>T (PRSS23)
NR_120591.2:n.1551G>T (PRSS23)
NR_120592.2:n.1300G>T (PRSS23)
NM_012193.4:c.568C>A (FZD4) MANE Select NP_036325.2:p.Gln190Lys
NR_120591.3:n.1551G>T (PRSS23)