Canonical Allele Identifier: CA1988808951

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952140_86952141delinsAG , CM000673.2:g.86952140_86952141delinsAG GRCh38
NC_000011.9:g.86663182_86663183delinsAG , CM000673.1:g.86663182_86663183delinsAG GRCh37
NC_000011.8:g.86340830_86340831delinsAG NCBI36
NG_011752.1:g.8251_8252delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.615_616delinsCT (FZD4) MANE Select ENSP00000434034.1:p.Gly205=
ENST00000531380.1:c.615_616delinsCT (FZD4) ENSP00000434034.1:p.Gly205=
ENST00000532234.5:c.*1133_*1134delinsAG (PRSS23) ENSP00000436676.1:n.*1133_*1134delinsAG
ENST00000533902.2:c.*855_*856delinsAG (PRSS23) ENSP00000437268.1:n.*855_*856delinsAG
NM_012193.3:c.615_616delinsCT (FZD4) NP_036325.2:p.Gly205=
NR_120591.1:n.1805_1806delinsAG (PRSS23)
NR_120592.1:n.1554_1555delinsAG (PRSS23)
NR_120591.2:n.1503_1504delinsAG (PRSS23)
NR_120592.2:n.1252_1253delinsAG (PRSS23)
NM_012193.4:c.615_616delinsCT (FZD4) MANE Select NP_036325.2:p.Gly205=
NR_120591.3:n.1503_1504delinsAG (PRSS23)