Canonical Allele Identifier: CA1335308058
Gene: PRSS56 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523750_232523751delinsAC , CM000664.2:g.232523750_232523751delinsAC GRCh38
NC_000002.11:g.233388460_233388461delinsAC , CM000664.1:g.233388460_233388461delinsAC GRCh37
NC_000002.10:g.233096704_233096705delinsAC NCBI36
NG_008028.1:g.2539_2540delinsAC
NG_031969.1:g.8288_8289delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.1013-22_1013-21delinsAC MANE Select ENSP00000479745.1:n.1013-22_1013-21delinsAC
ENST00000449534.6:c.1013-19_1013-18delinsAC ENSP00000473410.1:n.1013-19_1013-18delinsAC
ENST00000617714.1:c.1013-22_1013-21delinsAC ENSP00000479745.1:n.1013-22_1013-21delinsAC
NM_001195129.1:c.1013-22_1013-21delinsAC NP_001182058.1:n.1013-22_1013-21delinsAC
NM_001195129.2:c.1013-22_1013-21delinsAC MANE Select NP_001182058.1:n.1013-22_1013-21delinsAC
NM_001369848.1:c.1013-19_1013-18delinsAC NP_001356777.1:n.1013-19_1013-18delinsAC