Canonical Allele Identifier: CA369609007

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459806C>A (hg19) ; chr7:g.142751955C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751955C>A , CM000669.2:g.142751955C>A	GRCh38
NC_000007.13:g.142459806C>A , CM000669.1:g.142459806C>A	GRCh37
NC_000007.12:g.142139380C>A	NCBI36
NG_008307.3:g.7472C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.382C>A (PRSS1) MANE Select	ENSP00000308720.7:p.Leu128Met
ENST00000311737.11:c.382C>A (PRSS1)	ENSP00000308720.7:p.Leu128Met
ENST00000463701.1:n.846C>A (PRSS1)
ENST00000485223.1:n.1380C>A (PRSS1)
ENST00000486171.5:c.424C>A (PRSS1)	ENSP00000417854.1:p.Leu142Met
ENST00000492062.1:c.232C>A (PRSS1)	ENSP00000419912.1:p.Leu78Met
ENST00000610416.2:c.370+30769C>A (TRBC1)	ENSP00000482915.1:n.370+30769C>A
ENST00000612126.4:c.382C>A (PRSS1)	ENSP00000479959.1:p.Leu128Met
ENST00000619214.4:c.352C>A (PRSS1)	ENSP00000481361.1:p.Leu118Met
ENST00000633114.1:c.321+61C>A (PRSS2)	ENSP00000487822.1:n.321+61C>A
ENST00000634019.1:c.82+3164C>A (PRSS2)	ENSP00000488594.1:n.82+3164C>A
NM_002769.4:c.382C>A (PRSS1)	NP_002760.1:p.Leu128Met
XM_011516411.1:c.1057C>A (PRSS1)	XP_011514713.1:p.Leu353Met
NM_002769.5:c.382C>A (PRSS1) MANE Select	NP_002760.1:p.Leu128Met
NR_172947.1:n.324C>A (PRSS1)
NR_172948.1:n.321C>A (PRSS1)
NR_172949.1:n.321C>A (PRSS1)
NR_172950.1:n.235C>A (PRSS1)
NR_172951.1:n.169C>A (PRSS1)