Canonical Allele Identifier: CA369609089

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459831G>A (hg19) ; chr7:g.142751980G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751980G>A , CM000669.2:g.142751980G>A	GRCh38
NC_000007.13:g.142459831G>A , CM000669.1:g.142459831G>A	GRCh37
NC_000007.12:g.142139405G>A	NCBI36
NG_008307.3:g.7497G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000311737.12:c.407G>A (PRSS1) MANE Select	ENSP00000308720.7:p.Gly136Asp
ENST00000311737.11:c.407G>A (PRSS1)	ENSP00000308720.7:p.Gly136Asp
ENST00000463701.1:n.871G>A (PRSS1)
ENST00000485223.1:n.1405G>A (PRSS1)
ENST00000486171.5:c.449G>A (PRSS1)	ENSP00000417854.1:p.Gly150Asp
ENST00000492062.1:c.257G>A (PRSS1)	ENSP00000419912.1:p.Gly86Asp
ENST00000610416.2:c.370+30794G>A (TRBC1)	ENSP00000482915.1:n.370+30794G>A
ENST00000612126.4:c.407G>A (PRSS1)	ENSP00000479959.1:p.Gly136Asp
ENST00000619214.4:c.377G>A (PRSS1)	ENSP00000481361.1:p.Gly126Asp
ENST00000633114.1:c.321+86G>A (PRSS2)	ENSP00000487822.1:n.321+86G>A
ENST00000634019.1:c.82+3189G>A (PRSS2)	ENSP00000488594.1:n.82+3189G>A
NM_002769.4:c.407G>A (PRSS1)	NP_002760.1:p.Gly136Asp
XM_011516411.1:c.1082G>A (PRSS1)	XP_011514713.1:p.Gly361Asp
NM_002769.5:c.407G>A (PRSS1) MANE Select	NP_002760.1:p.Gly136Asp
NR_172947.1:n.349G>A (PRSS1)
NR_172948.1:n.346G>A (PRSS1)
NR_172949.1:n.346G>A (PRSS1)
NR_172950.1:n.260G>A (PRSS1)
NR_172951.1:n.194G>A (PRSS1)