Canonical Allele Identifier: CA369609249

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459871C>G (hg19) ; chr7:g.142752020C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142752020C>G , CM000669.2:g.142752020C>G	GRCh38
NC_000007.13:g.142459871C>G , CM000669.1:g.142459871C>G	GRCh37
NC_000007.12:g.142139445C>G	NCBI36
NG_008307.3:g.7537C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.447C>G (PRSS1) MANE Select	ENSP00000308720.7:p.Ser149Arg
ENST00000311737.11:c.447C>G (PRSS1)	ENSP00000308720.7:p.Ser149Arg
ENST00000463701.1:n.911C>G (PRSS1)
ENST00000486171.5:c.489C>G (PRSS1)	ENSP00000417854.1:p.Ser163Arg
ENST00000492062.1:c.297C>G (PRSS1)	ENSP00000419912.1:p.Ser99Arg
ENST00000610416.2:c.370+30834C>G (TRBC1)	ENSP00000482915.1:n.370+30834C>G
ENST00000612126.4:c.447C>G (PRSS1)	ENSP00000479959.1:p.Ser149Arg
ENST00000619214.4:c.417C>G (PRSS1)	ENSP00000481361.1:p.Ser139Arg
ENST00000633114.1:c.321+126C>G (PRSS2)	ENSP00000487822.1:n.321+126C>G
ENST00000634019.1:c.82+3229C>G (PRSS2)	ENSP00000488594.1:n.82+3229C>G
NM_002769.4:c.447C>G (PRSS1)	NP_002760.1:p.Ser149Arg
XM_011516411.1:c.1122C>G (PRSS1)	XP_011514713.1:p.Ser374Arg
NM_002769.5:c.447C>G (PRSS1) MANE Select	NP_002760.1:p.Ser149Arg
NR_172947.1:n.389C>G (PRSS1)
NR_172948.1:n.386C>G (PRSS1)
NR_172949.1:n.386C>G (PRSS1)
NR_172950.1:n.300C>G (PRSS1)
NR_172951.1:n.234C>G (PRSS1)