Canonical Allele Identifier: CA369608784

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459740A>C (hg19) ; chr7:g.142751889A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751889A>C , CM000669.2:g.142751889A>C	GRCh38
NC_000007.13:g.142459740A>C , CM000669.1:g.142459740A>C	GRCh37
NC_000007.12:g.142139314A>C	NCBI36
NG_008307.3:g.7406A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.316A>C (PRSS1) MANE Select	ENSP00000308720.7:p.Asn106His
ENST00000311737.11:c.316A>C (PRSS1)	ENSP00000308720.7:p.Asn106His
ENST00000463701.1:n.780A>C (PRSS1)
ENST00000485223.1:n.1314A>C (PRSS1)
ENST00000486171.5:c.358A>C (PRSS1)	ENSP00000417854.1:p.Asn120His
ENST00000492062.1:c.166A>C (PRSS1)	ENSP00000419912.1:p.Asn56His
ENST00000610416.2:c.370+30703A>C (TRBC1)	ENSP00000482915.1:n.370+30703A>C
ENST00000612126.4:c.316A>C (PRSS1)	ENSP00000479959.1:p.Asn106His
ENST00000619214.4:c.286A>C (PRSS1)	ENSP00000481361.1:p.Asn96His
ENST00000633114.1:c.316A>C (PRSS2)	ENSP00000487822.1:p.Asn106His
ENST00000634019.1:c.82+3098A>C (PRSS2)	ENSP00000488594.1:n.82+3098A>C
NM_002769.4:c.316A>C (PRSS1)	NP_002760.1:p.Asn106His
XM_011516411.1:c.991A>C (PRSS1)	XP_011514713.1:p.Asn331His
NM_002769.5:c.316A>C (PRSS1) MANE Select	NP_002760.1:p.Asn106His
NR_172947.1:n.258A>C (PRSS1)
NR_172948.1:n.255A>C (PRSS1)
NR_172949.1:n.255A>C (PRSS1)
NR_172950.1:n.169A>C (PRSS1)
NR_172951.1:n.140-37A>C (PRSS1)