Canonical Allele Identifier: CA458538207

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459631C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751780C>T , CM000669.2:g.142751780C>T	GRCh38
NC_000007.13:g.142459631C>T , CM000669.1:g.142459631C>T	GRCh37
NC_000007.12:g.142139205C>T	NCBI36
NG_008307.3:g.7297C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.207C>T (PRSS1) MANE Select	ENSP00000308720.7:p.Ile69=
ENST00000311737.11:c.207C>T (PRSS1)	ENSP00000308720.7:p.Ile69=
ENST00000463701.1:n.671C>T (PRSS1)
ENST00000485223.1:n.1205C>T (PRSS1)
ENST00000486171.5:c.249C>T (PRSS1)	ENSP00000417854.1:p.Ile83=
ENST00000492062.1:c.57C>T (PRSS1)	ENSP00000419912.1:p.Ile19=
ENST00000610416.2:c.370+30594C>T (TRBC1)	ENSP00000482915.1:n.370+30594C>T
ENST00000612126.4:c.207C>T (PRSS1)	ENSP00000479959.1:p.Ile69=
ENST00000619214.4:c.207C>T (PRSS1)	ENSP00000481361.1:p.Ile69=
ENST00000633114.1:c.207C>T (PRSS2)	ENSP00000487822.1:p.Ile69=
ENST00000634019.1:c.82+2989C>T (PRSS2)	ENSP00000488594.1:n.82+2989C>T
NM_002769.4:c.207C>T (PRSS1)	NP_002760.1:p.Ile69=
XM_011516411.1:c.882C>T (PRSS1)	XP_011514713.1:p.Ile294=
NM_002769.5:c.207C>T (PRSS1) MANE Select	NP_002760.1:p.Ile69=
NR_172947.1:n.198-49C>T (PRSS1)
NR_172948.1:n.198-52C>T (PRSS1)
NR_172949.1:n.146C>T (PRSS1)
NR_172950.1:n.60C>T (PRSS1)
NR_172951.1:n.140-146C>T (PRSS1)