Canonical Allele Identifier: CA369608934

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459784C>G (hg19) ; chr7:g.142751933C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751933C>G , CM000669.2:g.142751933C>G	GRCh38
NC_000007.13:g.142459784C>G , CM000669.1:g.142459784C>G	GRCh37
NC_000007.12:g.142139358C>G	NCBI36
NG_008307.3:g.7450C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.360C>G (PRSS1) MANE Select	ENSP00000308720.7:p.Asn120Lys
ENST00000311737.11:c.360C>G (PRSS1)	ENSP00000308720.7:p.Asn120Lys
ENST00000463701.1:n.824C>G (PRSS1)
ENST00000485223.1:n.1358C>G (PRSS1)
ENST00000486171.5:c.402C>G (PRSS1)	ENSP00000417854.1:p.Asn134Lys
ENST00000492062.1:c.210C>G (PRSS1)	ENSP00000419912.1:p.Asn70Lys
ENST00000610416.2:c.370+30747C>G (TRBC1)	ENSP00000482915.1:n.370+30747C>G
ENST00000612126.4:c.360C>G (PRSS1)	ENSP00000479959.1:p.Asn120Lys
ENST00000619214.4:c.330C>G (PRSS1)	ENSP00000481361.1:p.Asn110Lys
ENST00000633114.1:c.321+39C>G (PRSS2)	ENSP00000487822.1:n.321+39C>G
ENST00000634019.1:c.82+3142C>G (PRSS2)	ENSP00000488594.1:n.82+3142C>G
NM_002769.4:c.360C>G (PRSS1)	NP_002760.1:p.Asn120Lys
XM_011516411.1:c.1035C>G (PRSS1)	XP_011514713.1:p.Asn345Lys
NM_002769.5:c.360C>G (PRSS1) MANE Select	NP_002760.1:p.Asn120Lys
NR_172947.1:n.302C>G (PRSS1)
NR_172948.1:n.299C>G (PRSS1)
NR_172949.1:n.299C>G (PRSS1)
NR_172950.1:n.213C>G (PRSS1)
NR_172951.1:n.147C>G (PRSS1)