Canonical Allele Identifier: CA369608942

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459786C>G (hg19) ; chr7:g.142751935C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751935C>G , CM000669.2:g.142751935C>G	GRCh38
NC_000007.13:g.142459786C>G , CM000669.1:g.142459786C>G	GRCh37
NC_000007.12:g.142139360C>G	NCBI36
NG_008307.3:g.7452C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.362C>G (PRSS1) MANE Select	ENSP00000308720.7:p.Ala121Gly
ENST00000311737.11:c.362C>G (PRSS1)	ENSP00000308720.7:p.Ala121Gly
ENST00000463701.1:n.826C>G (PRSS1)
ENST00000485223.1:n.1360C>G (PRSS1)
ENST00000486171.5:c.404C>G (PRSS1)	ENSP00000417854.1:p.Ala135Gly
ENST00000492062.1:c.212C>G (PRSS1)	ENSP00000419912.1:p.Ala71Gly
ENST00000610416.2:c.370+30749C>G (TRBC1)	ENSP00000482915.1:n.370+30749C>G
ENST00000612126.4:c.362C>G (PRSS1)	ENSP00000479959.1:p.Ala121Gly
ENST00000619214.4:c.332C>G (PRSS1)	ENSP00000481361.1:p.Ala111Gly
ENST00000633114.1:c.321+41C>G (PRSS2)	ENSP00000487822.1:n.321+41C>G
ENST00000634019.1:c.82+3144C>G (PRSS2)	ENSP00000488594.1:n.82+3144C>G
NM_002769.4:c.362C>G (PRSS1)	NP_002760.1:p.Ala121Gly
XM_011516411.1:c.1037C>G (PRSS1)	XP_011514713.1:p.Ala346Gly
NM_002769.5:c.362C>G (PRSS1) MANE Select	NP_002760.1:p.Ala121Gly
NR_172947.1:n.304C>G (PRSS1)
NR_172948.1:n.301C>G (PRSS1)
NR_172949.1:n.301C>G (PRSS1)
NR_172950.1:n.215C>G (PRSS1)
NR_172951.1:n.149C>G (PRSS1)