Canonical Allele Identifier: CA2685349149

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v4: 7-142752035-G-GAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752035_142752036insAAA , CM000669.2:g.142752035_142752036insAAA	GRCh38
NC_000007.13:g.142459886_142459887insAAA , CM000669.1:g.142459886_142459887insAAA	GRCh37
NC_000007.12:g.142139460_142139461insAAA	NCBI36
NG_008307.3:g.7552_7553insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.454+8_454+9insAAA (PRSS1) MANE Select	ENSP00000308720.7:n.454+8_454+9insAAA
ENST00000311737.11:c.454+8_454+9insAAA (PRSS1)	ENSP00000308720.7:n.454+8_454+9insAAA
ENST00000463701.1:n.918+8_918+9insAAA (PRSS1)
ENST00000486171.5:c.496+8_496+9insAAA (PRSS1)	ENSP00000417854.1:n.496+8_496+9insAAA
ENST00000492062.1:c.304+8_304+9insAAA (PRSS1)	ENSP00000419912.1:n.304+8_304+9insAAA
ENST00000610416.2:c.370+30849_370+30850insAAA (TRBC1)	ENSP00000482915.1:n.370+30849_370+30850insAAA
ENST00000612126.4:c.454+8_454+9insAAA (PRSS1)	ENSP00000479959.1:n.454+8_454+9insAAA
ENST00000619214.4:c.424+8_424+9insAAA (PRSS1)	ENSP00000481361.1:n.424+8_424+9insAAA
ENST00000633114.1:c.321+141_321+142insAAA (PRSS2)	ENSP00000487822.1:n.321+141_321+142insAAA
ENST00000634019.1:c.82+3244_82+3245insAAA (PRSS2)	ENSP00000488594.1:n.82+3244_82+3245insAAA
NM_002769.4:c.454+8_454+9insAAA (PRSS1)	NP_002760.1:n.454+8_454+9insAAA
XM_011516411.1:c.1129+8_1129+9insAAA (PRSS1)	XP_011514713.1:n.1129+8_1129+9insAAA
NM_002769.5:c.454+8_454+9insAAA (PRSS1) MANE Select	NP_002760.1:n.454+8_454+9insAAA
NR_172947.1:n.396+8_396+9insAAA (PRSS1)
NR_172948.1:n.393+8_393+9insAAA (PRSS1)
NR_172949.1:n.393+8_393+9insAAA (PRSS1)
NR_172950.1:n.307+8_307+9insAAA (PRSS1)
NR_172951.1:n.241+8_241+9insAAA (PRSS1)