Canonical Allele Identifier: CA2577277633
Gene: PRSS56 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523718G>A , CM000664.2:g.232523718G>A GRCh38
NC_000002.11:g.233388428G>A , CM000664.1:g.233388428G>A GRCh37
NC_000002.10:g.233096672G>A NCBI36
NG_008028.1:g.2507G>A
NG_031969.1:g.8256G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.1013-54G>A MANE Select ENSP00000479745.1:n.1013-54G>A
ENST00000449534.6:c.1013-51G>A ENSP00000473410.1:n.1013-51G>A
ENST00000617714.1:c.1013-54G>A ENSP00000479745.1:n.1013-54G>A
NM_001195129.1:c.1013-54G>A NP_001182058.1:n.1013-54G>A
NM_001195129.2:c.1013-54G>A MANE Select NP_001182058.1:n.1013-54G>A
NM_001369848.1:c.1013-51G>A NP_001356777.1:n.1013-51G>A
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