Canonical Allele Identifier: CA2685351620

Gene: PRSS2 TRBC1

Linked Data

• gnomAD v4: 7-142774152-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142774154_142774155dup , CM000669.2:g.142774154_142774155dup	GRCh38
NC_000007.13:g.142482013_142482014dup , CM000669.1:g.142482013_142482014dup	GRCh37
NC_000007.12:g.142181957_142181958dup	NCBI36
NG_008322.2:g.8212_8213dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539842.6:c.591+99_591+100dup (PRSS2) MANE Select	ENSP00000488338.1:n.591+99_591+100dup
ENST00000539842.5:c.591+99_591+100dup (PRSS2)	ENSP00000488338.1:n.591+99_591+100dup
ENST00000610416.2:c.371-12884_371-12883dup (TRBC1)	ENSP00000482915.1:n.371-12884_371-12883dup
ENST00000618750.2:n.424+116_424+117dup (PRSS2)
ENST00000632805.1:c.588+99_588+100dup (PRSS2)	ENSP00000488077.1:n.588+99_588+100dup
ENST00000632998.1:c.591+99_591+100dup (PRSS2)	ENSP00000488789.1:n.591+99_591+100dup
ENST00000633114.1:c.597+99_597+100dup (PRSS2)	ENSP00000487822.1:n.597+99_597+100dup
ENST00000633969.1:c.633+99_633+100dup (PRSS2)	ENSP00000488437.1:n.633+99_633+100dup
ENST00000634019.1:c.633+99_633+100dup (PRSS2)	ENSP00000488594.1:n.633+99_633+100dup
NM_001303414.1:c.633+99_633+100dup (PRSS2)	NP_001290343.1:n.633+99_633+100dup
NM_002770.3:c.591+99_591+100dup (PRSS2)	NP_002761.1:n.591+99_591+100dup
NR_130149.1:n.557+99_557+100dup (PRSS2)
NM_002770.4:c.591+99_591+100dup (PRSS2) MANE Select	NP_002761.1:n.591+99_591+100dup
NR_130149.2:n.530+99_530+100dup (PRSS2)
NM_001303414.2:c.633+99_633+100dup (PRSS2)	NP_001290343.1:n.633+99_633+100dup