Canonical Allele Identifier: CA350992397

Gene: PRSS56

Linked Data

• MyVariant Identifiers: chr2:g.233388552C>G (hg19) ; chr2:g.232523842C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232523842C>G , CM000664.2:g.232523842C>G	GRCh38
NC_000002.11:g.233388552C>G , CM000664.1:g.233388552C>G	GRCh37
NC_000002.10:g.233096796C>G	NCBI36
NG_008028.1:g.2631C>G
NG_031969.1:g.8380C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617714.2:c.1083C>G MANE Select	ENSP00000479745.1:p.Asp361Glu
ENST00000449534.6:c.1086C>G	ENSP00000473410.1:p.Asp362Glu
ENST00000617714.1:c.1083C>G	ENSP00000479745.1:p.Asp361Glu
NM_001195129.1:c.1083C>G	NP_001182058.1:p.Asp361Glu
NM_001195129.2:c.1083C>G MANE Select	NP_001182058.1:p.Asp361Glu
NM_001369848.1:c.1086C>G	NP_001356777.1:p.Asp362Glu