Canonical Allele Identifier: CA369608613

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459698A>C (hg19) ; chr7:g.142751847A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751847A>C , CM000669.2:g.142751847A>C	GRCh38
NC_000007.13:g.142459698A>C , CM000669.1:g.142459698A>C	GRCh37
NC_000007.12:g.142139272A>C	NCBI36
NG_008307.3:g.7364A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.274A>C (PRSS1) MANE Select	ENSP00000308720.7:p.Lys92Gln
ENST00000311737.11:c.274A>C (PRSS1)	ENSP00000308720.7:p.Lys92Gln
ENST00000463701.1:n.738A>C (PRSS1)
ENST00000485223.1:n.1272A>C (PRSS1)
ENST00000486171.5:c.316A>C (PRSS1)	ENSP00000417854.1:p.Lys106Gln
ENST00000492062.1:c.124A>C (PRSS1)	ENSP00000419912.1:p.Lys42Gln
ENST00000610416.2:c.370+30661A>C (TRBC1)	ENSP00000482915.1:n.370+30661A>C
ENST00000612126.4:c.274A>C (PRSS1)	ENSP00000479959.1:p.Lys92Gln
ENST00000619214.4:c.244A>C (PRSS1)	ENSP00000481361.1:p.Lys82Gln
ENST00000633114.1:c.274A>C (PRSS2)	ENSP00000487822.1:p.Lys92Gln
ENST00000634019.1:c.82+3056A>C (PRSS2)	ENSP00000488594.1:n.82+3056A>C
NM_002769.4:c.274A>C (PRSS1)	NP_002760.1:p.Lys92Gln
XM_011516411.1:c.949A>C (PRSS1)	XP_011514713.1:p.Lys317Gln
NM_002769.5:c.274A>C (PRSS1) MANE Select	NP_002760.1:p.Lys92Gln
NR_172947.1:n.216A>C (PRSS1)
NR_172948.1:n.213A>C (PRSS1)
NR_172949.1:n.213A>C (PRSS1)
NR_172950.1:n.127A>C (PRSS1)
NR_172951.1:n.140-79A>C (PRSS1)