Canonical Allele Identifier: CA2685349587

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v4: 7-142752135-GAGTGCCCATTACACAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752138_142752153del , CM000669.2:g.142752138_142752153del	GRCh38
NC_000007.13:g.142459989_142460004del , CM000669.1:g.142459989_142460004del	GRCh37
NC_000007.12:g.142139563_142139578del	NCBI36
NG_008307.3:g.7655_7670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.454+111_454+126del (PRSS1) MANE Select	ENSP00000308720.7:n.454+111_454+126del
ENST00000311737.11:c.454+111_454+126del (PRSS1)	ENSP00000308720.7:n.454+111_454+126del
ENST00000463701.1:n.918+111_918+126del (PRSS1)
ENST00000486171.5:c.496+111_496+126del (PRSS1)	ENSP00000417854.1:n.496+111_496+126del
ENST00000492062.1:c.304+111_304+126del (PRSS1)	ENSP00000419912.1:n.304+111_304+126del
ENST00000610416.2:c.370+30952_370+30967del (TRBC1)	ENSP00000482915.1:n.370+30952_370+30967del
ENST00000612126.4:c.454+111_454+126del (PRSS1)	ENSP00000479959.1:n.454+111_454+126del
ENST00000619214.4:c.424+111_424+126del (PRSS1)	ENSP00000481361.1:n.424+111_424+126del
ENST00000633114.1:c.321+244_321+259del (PRSS2)	ENSP00000487822.1:n.321+244_321+259del
ENST00000634019.1:c.82+3347_82+3362del (PRSS2)	ENSP00000488594.1:n.82+3347_82+3362del
NM_002769.4:c.454+111_454+126del (PRSS1)	NP_002760.1:n.454+111_454+126del
XM_011516411.1:c.1129+111_1129+126del (PRSS1)	XP_011514713.1:n.1129+111_1129+126del
NM_002769.5:c.454+111_454+126del (PRSS1) MANE Select	NP_002760.1:n.454+111_454+126del
NR_172947.1:n.396+111_396+126del (PRSS1)
NR_172948.1:n.393+111_393+126del (PRSS1)
NR_172949.1:n.393+111_393+126del (PRSS1)
NR_172950.1:n.307+111_307+126del (PRSS1)
NR_172951.1:n.241+111_241+126del (PRSS1)