Canonical Allele Identifier: CA1335307983
Gene: PRSS56 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523605T= , CM000664.2:g.232523605T= GRCh38
NC_000002.11:g.233388315T= , CM000664.1:g.233388315T= GRCh37
NC_000002.10:g.233096559T= NCBI36
NG_008028.1:g.2394T=
NG_031969.1:g.8143T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.1012+27T= MANE Select ENSP00000479745.1:n.1012+27T=
ENST00000449534.6:c.1012+27T= ENSP00000473410.1:n.1012+27T=
ENST00000617714.1:c.1012+27T= ENSP00000479745.1:n.1012+27T=
NM_001195129.1:c.1012+27T= NP_001182058.1:n.1012+27T=
NM_001195129.2:c.1012+27T= MANE Select NP_001182058.1:n.1012+27T=
NM_001369848.1:c.1012+27T= NP_001356777.1:n.1012+27T=
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