Canonical Allele Identifier: CA1335308023
Gene: PRSS56 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523698T= , CM000664.2:g.232523698T= GRCh38
NC_000002.11:g.233388408T= , CM000664.1:g.233388408T= GRCh37
NC_000002.10:g.233096652T= NCBI36
NG_008028.1:g.2487T=
NG_031969.1:g.8236T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.1013-74T= MANE Select ENSP00000479745.1:n.1013-74T=
ENST00000449534.6:c.1013-71T= ENSP00000473410.1:n.1013-71T=
ENST00000617714.1:c.1013-74T= ENSP00000479745.1:n.1013-74T=
NM_001195129.1:c.1013-74T= NP_001182058.1:n.1013-74T=
NM_001195129.2:c.1013-74T= MANE Select NP_001182058.1:n.1013-74T=
NM_001369848.1:c.1013-71T= NP_001356777.1:n.1013-71T=