Canonical Allele Identifier: CA2793028904

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951429_86951454dup , CM000673.2:g.86951429_86951454dup GRCh38
NC_000011.9:g.86662471_86662496dup , CM000673.1:g.86662471_86662496dup GRCh37
NC_000011.8:g.86340119_86340144dup NCBI36
NG_011752.1:g.8938_8963dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1302_1327dup (FZD4) MANE Select ENSP00000434034.1:p.Leu443ArgfsTer18
ENST00000531380.1:c.1302_1327dup (FZD4) ENSP00000434034.1:p.Leu443ArgfsTer18
ENST00000531521.1:n.600_625dup (PRSS23)
ENST00000532234.5:c.*422_*447dup (PRSS23) ENSP00000436676.1:n.*422_*447dup
ENST00000533902.2:c.*144_*169dup (PRSS23) ENSP00000437268.1:n.*144_*169dup
NM_012193.3:c.1302_1327dup (FZD4) NP_036325.2:p.Leu443ArgfsTer18
NR_120591.1:n.1094_1119dup (PRSS23)
NR_120592.1:n.843_868dup (PRSS23)
NR_120591.2:n.792_817dup (PRSS23)
NR_120592.2:n.541_566dup (PRSS23)
NM_012193.4:c.1302_1327dup (FZD4) MANE Select NP_036325.2:p.Leu443ArgfsTer18
NR_120591.3:n.792_817dup (PRSS23)