Canonical Allele Identifier: CA476145158

Linked Data

MyVariant Identifiers: chr11:g.86663408G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952366G>T , CM000673.2:g.86952366G>T GRCh38
NC_000011.9:g.86663408G>T , CM000673.1:g.86663408G>T GRCh37
NC_000011.8:g.86341056G>T NCBI36
NG_011752.1:g.8026C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.390C>A (FZD4) MANE Select ENSP00000434034.1:p.Pro130=
ENST00000531380.1:c.390C>A (FZD4) ENSP00000434034.1:p.Pro130=
ENST00000532234.5:c.*1359G>T (PRSS23) ENSP00000436676.1:n.*1359G>T
ENST00000533902.2:c.*1081G>T (PRSS23) ENSP00000437268.1:n.*1081G>T
NM_012193.3:c.390C>A (FZD4) NP_036325.2:p.Pro130=
NR_120591.1:n.2031G>T (PRSS23)
NR_120592.1:n.1780G>T (PRSS23)
NR_120591.2:n.1729G>T (PRSS23)
NR_120592.2:n.1478G>T (PRSS23)
NM_012193.4:c.390C>A (FZD4) MANE Select NP_036325.2:p.Pro130=
NR_120591.3:n.1729G>T (PRSS23)