Canonical Allele Identifier: CA350990884
Gene: PRSS56 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523466A>T , CM000664.2:g.232523466A>T GRCh38
NC_000002.11:g.233388176A>T , CM000664.1:g.233388176A>T GRCh37
NC_000002.10:g.233096420A>T NCBI36
NG_008028.1:g.2255A>T
NG_031969.1:g.8004A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.900A>T MANE Select ENSP00000479745.1:p.Arg300Ser
ENST00000449534.6:c.900A>T ENSP00000473410.1:p.Arg300Ser
ENST00000617714.1:c.900A>T ENSP00000479745.1:p.Arg300Ser
NM_001195129.1:c.900A>T NP_001182058.1:p.Arg300Ser
NM_001195129.2:c.900A>T MANE Select NP_001182058.1:p.Arg300Ser
NM_001369848.1:c.900A>T NP_001356777.1:p.Arg300Ser