Canonical Allele Identifier: CA369607059

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• ClinVar Variation Id: 1752175
• ClinVar RCV Id: RCV002366448
• MyVariant Identifiers: chr7:g.142458426G>C (hg19) ; chr7:g.142750575G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142750575G>C , CM000669.2:g.142750575G>C	GRCh38
NC_000007.13:g.142458426G>C , CM000669.1:g.142458426G>C	GRCh37
NC_000007.12:g.142138000G>C	NCBI36
NG_008307.3:g.6092G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.61G>C (PRSS1) MANE Select	ENSP00000308720.7:p.Asp21His
ENST00000311737.11:c.61G>C (PRSS1)	ENSP00000308720.7:p.Asp21His
ENST00000485223.1:n.54-54G>C (PRSS1)
ENST00000486171.5:c.61G>C (PRSS1)	ENSP00000417854.1:p.Asp21His
ENST00000497041.1:n.65G>C (PRSS1)
ENST00000610416.2:c.370+29389G>C (TRBC1)	ENSP00000482915.1:n.370+29389G>C
ENST00000612126.4:c.61G>C (PRSS1)	ENSP00000479959.1:p.Asp21His
ENST00000619214.4:c.61G>C (PRSS1)	ENSP00000481361.1:p.Asp21His
ENST00000633114.1:c.61G>C (PRSS2)	ENSP00000487822.1:p.Asp21His
ENST00000634019.1:c.82+1784G>C (PRSS2)	ENSP00000488594.1:n.82+1784G>C
NM_002769.4:c.61G>C (PRSS1)	NP_002760.1:p.Asp21His
XM_011516411.1:c.736G>C (PRSS1)	XP_011514713.1:p.Asp246His
NM_002769.5:c.61G>C (PRSS1) MANE Select	NP_002760.1:p.Asp21His
NR_172947.1:n.74G>C (PRSS1)
NR_172948.1:n.74G>C (PRSS1)
NR_172949.1:n.54-54G>C (PRSS1)
NR_172950.1:n.53+1051G>C (PRSS1)
NR_172951.1:n.54-54G>C (PRSS1)