Canonical Allele Identifier: CA2685351927

Gene: PRSS2 TRBC1

Linked Data

• gnomAD v4: 7-142774210-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142774210T>A , CM000669.2:g.142774210T>A	GRCh38
NC_000007.13:g.142482070T>A , CM000669.1:g.142482070T>A	GRCh37
NC_000007.12:g.142182013T>A	NCBI36
NG_008322.2:g.8268T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539842.6:c.592-146T>A (PRSS2) MANE Select	ENSP00000488338.1:n.592-146T>A
ENST00000539842.5:c.592-146T>A (PRSS2)	ENSP00000488338.1:n.592-146T>A
ENST00000610416.2:c.371-12828T>A (TRBC1)	ENSP00000482915.1:n.371-12828T>A
ENST00000618750.2:n.425-146T>A (PRSS2)
ENST00000632805.1:c.589-146T>A (PRSS2)	ENSP00000488077.1:n.589-146T>A
ENST00000632998.1:c.592-146T>A (PRSS2)	ENSP00000488789.1:n.592-146T>A
ENST00000633114.1:c.598-146T>A (PRSS2)	ENSP00000487822.1:n.598-146T>A
ENST00000633969.1:c.634-146T>A (PRSS2)	ENSP00000488437.1:n.634-146T>A
ENST00000634019.1:c.634-146T>A (PRSS2)	ENSP00000488594.1:n.634-146T>A
NM_001303414.1:c.634-146T>A (PRSS2)	NP_001290343.1:n.634-146T>A
NM_002770.3:c.592-146T>A (PRSS2)	NP_002761.1:n.592-146T>A
NR_130149.1:n.558-146T>A (PRSS2)
NM_002770.4:c.592-146T>A (PRSS2) MANE Select	NP_002761.1:n.592-146T>A
NR_130149.2:n.531-146T>A (PRSS2)
NM_001303414.2:c.634-146T>A (PRSS2)	NP_001290343.1:n.634-146T>A