Canonical Allele Identifier: CA2587779801
Gene: PRSS57 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.695061_695066del , CM000681.2:g.695061_695066del GRCh38
NC_000019.9:g.695061_695066del , CM000681.1:g.695061_695066del GRCh37
NC_000019.8:g.646061_646066del NCBI36
NG_051189.1:g.5472_5477del

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.80-93_80-88del MANE Select ENSP00000327386.6:n.80-93_80-88del
ENST00000329267.8:c.80-93_80-88del ENSP00000327386.6:n.80-93_80-88del
ENST00000613411.4:c.80-90_80-85del ENSP00000482358.1:n.80-90_80-85del
NM_001308209.1:c.80-93_80-88del NP_001295138.1:n.80-93_80-88del
NM_214710.3:c.80-90_80-85del NP_999875.1:n.80-90_80-85del
NM_214710.4:c.80-90_80-85del NP_999875.1:n.80-90_80-85del
NM_001308209.2:c.80-93_80-88del MANE Select NP_001295138.2:n.80-93_80-88del
NM_214710.5:c.80-90_80-85del NP_999875.2:n.80-90_80-85del