Canonical Allele Identifier: CA458538209

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• COSMIC: COSM3778181
• MyVariant Identifiers: chr7:g.142459637G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751786G>A , CM000669.2:g.142751786G>A	GRCh38
NC_000007.13:g.142459637G>A , CM000669.1:g.142459637G>A	GRCh37
NC_000007.12:g.142139211G>A	NCBI36
NG_008307.3:g.7303G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.213G>A (PRSS1) MANE Select	ENSP00000308720.7:p.Val71=
ENST00000311737.11:c.213G>A (PRSS1)	ENSP00000308720.7:p.Val71=
ENST00000463701.1:n.677G>A (PRSS1)
ENST00000485223.1:n.1211G>A (PRSS1)
ENST00000486171.5:c.255G>A (PRSS1)	ENSP00000417854.1:p.Val85=
ENST00000492062.1:c.63G>A (PRSS1)	ENSP00000419912.1:p.Val21=
ENST00000610416.2:c.370+30600G>A (TRBC1)	ENSP00000482915.1:n.370+30600G>A
ENST00000612126.4:c.213G>A (PRSS1)	ENSP00000479959.1:p.Val71=
ENST00000619214.4:c.213G>A (PRSS1)	ENSP00000481361.1:p.Val71=
ENST00000633114.1:c.213G>A (PRSS2)	ENSP00000487822.1:p.Val71=
ENST00000634019.1:c.82+2995G>A (PRSS2)	ENSP00000488594.1:n.82+2995G>A
NM_002769.4:c.213G>A (PRSS1)	NP_002760.1:p.Val71=
XM_011516411.1:c.888G>A (PRSS1)	XP_011514713.1:p.Val296=
NM_002769.5:c.213G>A (PRSS1) MANE Select	NP_002760.1:p.Val71=
NR_172947.1:n.198-43G>A (PRSS1)
NR_172948.1:n.198-46G>A (PRSS1)
NR_172949.1:n.152G>A (PRSS1)
NR_172950.1:n.66G>A (PRSS1)
NR_172951.1:n.140-140G>A (PRSS1)