Canonical Allele Identifier: CA834446792

Gene: TRBC1 PRSS1 PRSS2

Linked Data

• dbSNP Id: rs1443400695
• gnomAD v3: 7-142753941-C-CG
• gnomAD v4: 7-142753941-C-CG
• MyVariant Identifiers: chr7:g.142461792_142461793insG (hg19) ; chr7:g.142753941_142753942insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142753941_142753942insG , CM000669.2:g.142753941_142753942insG	GRCh38
NC_000007.13:g.142461792_142461793insG , CM000669.1:g.142461792_142461793insG	GRCh37
NC_000007.12:g.142141366_142141367insG	NCBI36
NG_008307.3:g.9458_9459insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610416.2:c.370+32755_370+32756insG (TRBC1)	ENSP00000482915.1:n.370+32755_370+32756insG
ENST00000612126.4:c.591+1374_591+1375insG (PRSS1)	ENSP00000479959.1:n.591+1374_591+1375insG
ENST00000633114.1:c.321+2047_321+2048insG (PRSS2)	ENSP00000487822.1:n.321+2047_321+2048insG
ENST00000634019.1:c.82+5150_82+5151insG (PRSS2)	ENSP00000488594.1:n.82+5150_82+5151insG