Canonical Allele Identifier: CA2778215844

Gene: PRSS1 TRBC1 PRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752085_142752086insA , CM000669.2:g.142752085_142752086insA	GRCh38
NC_000007.13:g.142459936_142459937insA , CM000669.1:g.142459936_142459937insA	GRCh37
NC_000007.12:g.142139510_142139511insA	NCBI36
NG_008307.3:g.7602_7603insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.454+58_454+59insA (PRSS1) MANE Select	ENSP00000308720.7:n.454+58_454+59insA
ENST00000311737.11:c.454+58_454+59insA (PRSS1)	ENSP00000308720.7:n.454+58_454+59insA
ENST00000463701.1:n.918+58_918+59insA (PRSS1)
ENST00000486171.5:c.496+58_496+59insA (PRSS1)	ENSP00000417854.1:n.496+58_496+59insA
ENST00000492062.1:c.304+58_304+59insA (PRSS1)	ENSP00000419912.1:n.304+58_304+59insA
ENST00000610416.2:c.370+30899_370+30900insA (TRBC1)	ENSP00000482915.1:n.370+30899_370+30900insA
ENST00000612126.4:c.454+58_454+59insA (PRSS1)	ENSP00000479959.1:n.454+58_454+59insA
ENST00000619214.4:c.424+58_424+59insA (PRSS1)	ENSP00000481361.1:n.424+58_424+59insA
ENST00000633114.1:c.321+191_321+192insA (PRSS2)	ENSP00000487822.1:n.321+191_321+192insA
ENST00000634019.1:c.82+3294_82+3295insA (PRSS2)	ENSP00000488594.1:n.82+3294_82+3295insA
NM_002769.4:c.454+58_454+59insA (PRSS1)	NP_002760.1:n.454+58_454+59insA
XM_011516411.1:c.1129+58_1129+59insA (PRSS1)	XP_011514713.1:n.1129+58_1129+59insA
NM_002769.5:c.454+58_454+59insA (PRSS1) MANE Select	NP_002760.1:n.454+58_454+59insA
NR_172947.1:n.396+58_396+59insA (PRSS1)
NR_172948.1:n.393+58_393+59insA (PRSS1)
NR_172949.1:n.393+58_393+59insA (PRSS1)
NR_172950.1:n.307+58_307+59insA (PRSS1)
NR_172951.1:n.241+58_241+59insA (PRSS1)