Canonical Allele Identifier: CA578433218

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• gnomAD v2: 7-142459878-G-GCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT
• MyVariant Identifiers: chr7:g.142459878_142459879insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (hg19) ; chr7:g.142752027_142752028insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752027_142752028insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT , CM000669.2:g.142752027_142752028insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT	GRCh38
NC_000007.13:g.142459878_142459879insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT , CM000669.1:g.142459878_142459879insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT	GRCh37
NC_000007.12:g.142139452_142139453insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT	NCBI36
NG_008307.3:g.7544_7545insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.454_454+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1) MANE Select	ENSP00000308720.7:n.454_454+1insCCGACTACCCAGACGAGCTGCAGTGCCTG...
ENST00000311737.11:c.454_454+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)	ENSP00000308720.7:n.454_454+1insCCGACTACCCAGACGAGCTGCAGTGCCTG...
ENST00000463701.1:n.918_918+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)
ENST00000486171.5:c.496_496+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)	ENSP00000417854.1:n.496_496+1insCCGACTACCCAGACGAGCTGCAGTGCCTG...
ENST00000492062.1:c.304_304+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)	ENSP00000419912.1:n.304_304+1insCCGACTACCCAGACGAGCTGCAGTGCCTG...
ENST00000610416.2:c.370+30841_370+30842insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (TRBC1)	ENSP00000482915.1:n.370+30841_370+30842insCCGACTACCCAGACGAGCT...
ENST00000612126.4:c.454_454+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)	ENSP00000479959.1:n.454_454+1insCCGACTACCCAGACGAGCTGCAGTGCCTG...
ENST00000619214.4:c.424_424+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)	ENSP00000481361.1:n.424_424+1insCCGACTACCCAGACGAGCTGCAGTGCCTG...
ENST00000633114.1:c.321+133_321+134insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS2)	ENSP00000487822.1:n.321+133_321+134insCCGACTACCCAGACGAGCTGCAG...
ENST00000634019.1:c.82+3236_82+3237insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS2)	ENSP00000488594.1:n.82+3236_82+3237insCCGACTACCCAGACGAGCTGCAG...
NM_002769.4:c.454_454+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)	NP_002760.1:n.454_454+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCT...
XM_011516411.1:c.1129_1129+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)	XP_011514713.1:n.1129_1129+1insCCGACTACCCAGACGAGCTGCAGTGCCTGG...
NM_002769.5:c.454_454+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1) MANE Select	NP_002760.1:n.454_454+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCT...
NR_172947.1:n.396_396+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)
NR_172948.1:n.393_393+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)
NR_172949.1:n.393_393+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)
NR_172950.1:n.307_307+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)
NR_172951.1:n.241_241+1insCCGACTACCCAGACGAGCTGCAGTGCCTGGACGCTCCTGTGCT (PRSS1)