Canonical Allele Identifier: CA1748624191

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751818_142751819delinsAG , CM000669.2:g.142751818_142751819delinsAG	GRCh38
NC_000007.13:g.142459669_142459670delinsAG , CM000669.1:g.142459669_142459670delinsAG	GRCh37
NC_000007.12:g.142139243_142139244delinsAG	NCBI36
NG_008307.3:g.7335_7336delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.245_246delinsAG (PRSS1) MANE Select	ENSP00000308720.7:p.Glu82=
ENST00000311737.11:c.245_246delinsAG (PRSS1)	ENSP00000308720.7:p.Glu82=
ENST00000463701.1:n.709_710delinsAG (PRSS1)
ENST00000485223.1:n.1243_1244delinsAG (PRSS1)
ENST00000486171.5:c.287_288delinsAG (PRSS1)	ENSP00000417854.1:p.Glu96=
ENST00000492062.1:c.95_96delinsAG (PRSS1)	ENSP00000419912.1:p.Glu32=
ENST00000610416.2:c.370+30632_370+30633delinsAG (TRBC1)	ENSP00000482915.1:n.370+30632_370+30633delinsAG
ENST00000612126.4:c.245_246delinsAG (PRSS1)	ENSP00000479959.1:p.Glu82=
ENST00000619214.4:c.233+12_233+13delinsAG (PRSS1)	ENSP00000481361.1:n.233+12_233+13delinsAG
ENST00000633114.1:c.245_246delinsAG (PRSS2)	ENSP00000487822.1:p.Glu82=
ENST00000634019.1:c.82+3027_82+3028delinsAG (PRSS2)	ENSP00000488594.1:n.82+3027_82+3028delinsAG
NM_002769.4:c.245_246delinsAG (PRSS1)	NP_002760.1:p.Glu82=
XM_011516411.1:c.920_921delinsAG (PRSS1)	XP_011514713.1:p.Glu307=
NM_002769.5:c.245_246delinsAG (PRSS1) MANE Select	NP_002760.1:p.Glu82=
NR_172947.1:n.198-11_198-10delinsAG (PRSS1)
NR_172948.1:n.198-14_198-13delinsAG (PRSS1)
NR_172949.1:n.184_185delinsAG (PRSS1)
NR_172950.1:n.98_99delinsAG (PRSS1)
NR_172951.1:n.140-108_140-107delinsAG (PRSS1)